# Electronic Supplementary Material (ESI) for Organic Chemistry Frontiers.
# This journal is © the Partner Organisations 2015

####################################################################### 
# 
# This file contains crystal structure data downloaded from the 
# Cambridge Structural Database (CSD) hosted by the Cambridge 
# Crystallographic Data Centre (CCDC).
# 
# Full information about CCDC data access policies and citation 
# guidelines are available at http://www.ccdc.cam.ac.uk/access/V1 
# 
# Audit and citation data items may have been added by the CCDC. 
# Please retain this information to preserve the provenance of 
# this file and to allow appropriate attribution of the data. 
# 
#######################################################################

data_TNY-TE-09
_database_code_depnum_ccdc_archive 'CCDC 1050176'
_audit_update_record             
;
2015-02-18 deposited with the CCDC.
2015-11-16 downloaded from the CCDC.
;
_audit_creation_date             2015-02-17
_audit_creation_method           
;
  Olex2 1.2-ac2
  (compiled Nov  7 2012 10:34:12, GUI svn.r4372)
;
_chemical_name_common            TNY-TE-09
_chemical_name_systematic        
;
Benzoic acid 2-(cyclohexyl-phenyl-amino)-1-phenyl-ethyl ester
;
_chemical_formula_moiety         'C27 H29 N O2'
_chemical_formula_sum            'C27 H29 N O2'
_chemical_formula_weight         399.51
_chemical_melting_point          ?
loop_
_atom_type_symbol
_atom_type_description
_atom_type_scat_dispersion_real
_atom_type_scat_dispersion_imag
_atom_type_scat_source
C C 0.0033 0.0016 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
H H 0.0000 0.0000 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
N N 0.0061 0.0033 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'
O O 0.0106 0.0060 'International Tables Vol C Tables 4.2.6.8 and 6.1.1.4'

_space_group_crystal_system      monoclinic
_space_group_IT_number           14
_space_group_name_H-M_alt        'P 1 21/c 1'
_space_group_name_Hall           '-P 2ybc'
loop_
_space_group_symop_id
_space_group_symop_operation_xyz
1 'x, y, z'
2 '-x, y+1/2, -z+1/2'
3 '-x, -y, -z'
4 'x, -y-1/2, z-1/2'

_cell_length_a                   15.5737(5)
_cell_length_b                   12.7774(4)
_cell_length_c                   11.4615(3)
_cell_angle_alpha                90.00
_cell_angle_beta                 91.399(3)
_cell_angle_gamma                90.00
_cell_volume                     2280.08(12)
_cell_formula_units_Z            4
_cell_measurement_reflns_used    ?
_cell_measurement_temperature    298
_cell_measurement_theta_max      ?
_cell_measurement_theta_min      ?
_exptl_absorpt_coefficient_mu    0.072
_exptl_absorpt_correction_T_max  0.985
_exptl_absorpt_correction_T_min  0.982
_exptl_absorpt_correction_type   multi-scan
_exptl_absorpt_process_details   
;
CrysAlisPro, Agilent Technologies,
Version 1.171.37.33c (release 11-04-2014 CrysAlis171 .NET)
(compiled Apr 11 2014,15:12:41)
Empirical absorption correction using spherical harmonics,
 implemented in SCALE3 ABSPACK scaling algorithm.
;
_exptl_crystal_colour            'clear red'
_exptl_crystal_colour_lustre     clear
_exptl_crystal_colour_primary    red
_exptl_crystal_density_diffrn    1.164
_exptl_crystal_density_meas      ?
_exptl_crystal_density_method    'not measured'
_exptl_crystal_description       needle
_exptl_crystal_F_000             856
_exptl_crystal_size_max          0.4
_exptl_crystal_size_mid          0.2
_exptl_crystal_size_min          0.2
_exptl_special_details           
;
 ? 
;
_diffrn_reflns_av_R_equivalents  0.0280
_diffrn_reflns_av_unetI/netI     0.0404
_diffrn_reflns_limit_h_max       11
_diffrn_reflns_limit_h_min       -21
_diffrn_reflns_limit_k_max       16
_diffrn_reflns_limit_k_min       -4
_diffrn_reflns_limit_l_max       15
_diffrn_reflns_limit_l_min       -11
_diffrn_reflns_number            10221
_diffrn_reflns_theta_full        25.00
_diffrn_reflns_theta_max         29.01
_diffrn_reflns_theta_min         3.19
_diffrn_ambient_temperature      298
_diffrn_detector_area_resol_mean ?
_diffrn_measured_fraction_theta_full 0.998
_diffrn_measured_fraction_theta_max 0.875
_diffrn_measurement_device_type  ?
_diffrn_measurement_method       ?
_diffrn_radiation_monochromator  graphite
_diffrn_radiation_type           MoK\a
_diffrn_radiation_wavelength     0.71073
_diffrn_source                   'fine-focus sealed tube'
_diffrn_standards_decay_%        ?
_diffrn_standards_interval_count ?
_diffrn_standards_interval_time  ?
_diffrn_standards_number         ?
_reflns_number_gt                2970
_reflns_number_total             5313
_reflns_threshold_expression     >2sigma(I)
_computing_cell_refinement       ?
_computing_data_collection       ?
_computing_data_reduction        ?
_computing_molecular_graphics    
;
O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, J. A. K. Howard and H. Puschmann,
OLEX2: a complete structure solution, refinement and analysis program.
J. Appl. Cryst. (2009). 42, 339-341.
;
_computing_publication_material  
;
O. V. Dolomanov, L. J. Bourhis, R. J. Gildea, J. A. K. Howard and H. Puschmann,
OLEX2: a complete structure solution, refinement and analysis program.
J. Appl. Cryst. (2009). 42, 339-341.
;
_computing_structure_refinement  
;
SHELXL, G.M. Sheldrick, Acta Cryst.
(2008). A64, 112-122
;
_computing_structure_solution    
;
SHELXS, G.M. Sheldrick, Acta Cryst.
(2008). A64, 112-122
;
_refine_diff_density_max         0.336
_refine_diff_density_min         -0.152
_refine_diff_density_rms         0.036
_refine_ls_extinction_coef       ?
_refine_ls_extinction_method     none
_refine_ls_goodness_of_fit_ref   1.095
_refine_ls_hydrogen_treatment    mixed
_refine_ls_matrix_type           full
_refine_ls_number_parameters     271
_refine_ls_number_reflns         5313
_refine_ls_number_restraints     0
_refine_ls_R_factor_all          0.1180
_refine_ls_R_factor_gt           0.0678
_refine_ls_restrained_S_all      1.095
_refine_ls_shift/su_max          0.000
_refine_ls_shift/su_mean         0.000
_refine_ls_structure_factor_coef Fsqd
_refine_ls_weighting_details     
'calc w=1/[σ²(Fo²)+(0.0770P)²+0.6751P] where P=(Fo²+2Fc²)/3'
_refine_ls_weighting_scheme      calc
_refine_ls_wR_factor_gt          0.1884
_refine_ls_wR_factor_ref         0.2219
_refine_special_details          
;
 Refinement of F² against ALL reflections.  The weighted R-factor wR and 
 goodness of fit S are based on F², conventional R-factors R are based 
 on F, with F set to zero for negative F². The threshold expression of 
 F² > 2sigma(F²) is used only for calculating R-factors(gt) etc. and is 
 not relevant to the choice of reflections for refinement.  R-factors based 
 on F² are statistically about twice as large as those based on F, and R- 
 factors based on ALL data will be even larger. 
;
_olex2_refinement_description    
;
1. Fixed Uiso
 At 1.2 times of:
  H22 of C22, {H15a,H15b} of C15, {H27a,H27b} of C27, H8 of C8, H20 of C20,
  {H24a,H24b} of C24, H21 of C21, H17 of C17, H2 of C2, H11 of C11, {H26a,H26b}
  of C26, H5 of C5, {H23a,H23b} of C23, H14 of C14, H6 of C6, H10 of C10, H3 of
  C3, H4 of C4, H12 of C12, H18 of C18, H19 of C19, H13 of C13, {H25a,H25b} of
  C25
2.a Ternary CH refined with riding coordinates:
 C8(H8), C22(H22)
2.b Secondary CH2 refined with riding coordinates:
 C15(H15a,H15b), C27(H27a,H27b), C23(H23a,H23b), C26(H26a,H26b), C24(H24a,
 H24b), C25(H25a,H25b)
2.c Aromatic/amide H refined with riding coordinates:
 C6(H6), C17(H17), C21(H21), C14(H14), C2(H2), C10(H10), C5(H5), C11(H11),
 C20(H20), C12(H12), C13(H13), C18(H18), C3(H3), C4(H4), C19(H19)
;
_atom_sites_solution_hydrogens   geom
_atom_sites_solution_primary     direct
_atom_sites_solution_secondary   difmap
loop_
_atom_site_label
_atom_site_type_symbol
_atom_site_fract_x
_atom_site_fract_y
_atom_site_fract_z
_atom_site_U_iso_or_equiv
_atom_site_adp_type
_atom_site_occupancy
_atom_site_symmetry_multiplicity
_atom_site_calc_flag
_atom_site_refinement_flags
_atom_site_disorder_assembly
_atom_site_disorder_group
O2 O 0.16967(11) 0.22005(14) 0.12952(14) 0.0599(5) Uani 1 1 d . . .
C7 C 0.13037(16) 0.1868(2) 0.2247(2) 0.0572(6) Uani 1 1 d . . .
O1 O 0.15697(13) 0.11564(18) 0.28327(17) 0.0869(7) Uani 1 1 d . . .
N1 N 0.33048(14) 0.33269(17) 0.11223(16) 0.0604(6) Uani 1 1 d . . .
C1 C 0.05264(15) 0.2480(2) 0.2489(2) 0.0573(6) Uani 1 1 d . . .
C15 C 0.29965(17) 0.2503(2) 0.0351(2) 0.0592(6) Uani 1 1 d . . .
H15A H 0.3482 0.2171 -0.0013 0.071 Uiso 1 1 calc R . .
H15B H 0.2635 0.2805 -0.0262 0.071 Uiso 1 1 calc R . .
C27 C 0.37638(17) 0.4460(2) -0.0513(2) 0.0658(7) Uani 1 1 d . . .
H27A H 0.4347 0.4210 -0.0389 0.079 Uiso 1 1 calc R . .
H27B H 0.3484 0.4012 -0.1090 0.079 Uiso 1 1 calc R . .
C8 C 0.24889(15) 0.1682(2) 0.0999(2) 0.0557(6) Uani 1 1 d . . .
H8 H 0.2803 0.1481 0.1716 0.067 Uiso 1 1 calc R . .
C22 C 0.32906(16) 0.4389(2) 0.0619(2) 0.0569(6) Uani 1 1 d . . .
H22 H 0.3596 0.4844 0.1178 0.068 Uiso 1 1 calc R . .
C9 C 0.23165(16) 0.0730(2) 0.0266(2) 0.0572(6) Uani 1 1 d . . .
C16 C 0.39995(17) 0.3101(2) 0.1889(2) 0.0607(7) Uani 1 1 d . . .
C6 C 0.02804(18) 0.3333(2) 0.1829(2) 0.0701(7) Uani 1 1 d . . .
H6 H 0.0592 0.3520 0.1179 0.084 Uiso 1 1 calc R . .
C23 C 0.23921(18) 0.4821(2) 0.0476(3) 0.0766(8) Uani 1 1 d . . .
H23A H 0.2117 0.4829 0.1227 0.092 Uiso 1 1 calc R . .
H23B H 0.2057 0.4375 -0.0047 0.092 Uiso 1 1 calc R . .
C26 C 0.3785(2) 0.5567(3) -0.0967(3) 0.0876(10) Uani 1 1 d . . .
H26A H 0.4103 0.6006 -0.0418 0.105 Uiso 1 1 calc R . .
H26B H 0.4078 0.5581 -0.1704 0.105 Uiso 1 1 calc R . .
C17 C 0.4186(2) 0.3783(3) 0.2811(2) 0.0747(8) Uani 1 1 d . . .
H17 H 0.3843 0.4369 0.2919 0.090 Uiso 1 1 calc R . .
C21 C 0.45005(19) 0.2216(3) 0.1800(3) 0.0800(9) Uani 1 1 d . . .
H21 H 0.4383 0.1732 0.1213 0.096 Uiso 1 1 calc R . .
C14 C 0.1621(2) 0.0657(3) -0.0483(3) 0.0843(9) Uani 1 1 d . . .
H14 H 0.1223 0.1200 -0.0523 0.101 Uiso 1 1 calc R . .
C2 C 0.0055(2) 0.2209(3) 0.3444(3) 0.0821(9) Uani 1 1 d . . .
H2 H 0.0211 0.1628 0.3889 0.099 Uiso 1 1 calc R . .
C10 C 0.28868(19) -0.0087(2) 0.0305(3) 0.0746(8) Uani 1 1 d . . .
H10 H 0.3360 -0.0061 0.0815 0.090 Uiso 1 1 calc R . .
C5 C -0.0427(2) 0.3908(3) 0.2132(3) 0.0886(10) Uani 1 1 d . . .
H5 H -0.0595 0.4482 0.1683 0.106 Uiso 1 1 calc R . .
C11 C 0.2765(2) -0.0947(3) -0.0405(3) 0.0908(10) Uani 1 1 d . . .
H11 H 0.3162 -0.1491 -0.0374 0.109 Uiso 1 1 calc R . .
C20 C 0.5183(2) 0.2045(3) 0.2588(4) 0.1010(12) Uani 1 1 d . . .
H20 H 0.5514 0.1443 0.2520 0.121 Uiso 1 1 calc R . .
C24 C 0.2420(2) 0.5933(3) -0.0019(4) 0.0986(11) Uani 1 1 d . . .
H24A H 0.1838 0.6181 -0.0159 0.118 Uiso 1 1 calc R . .
H24B H 0.2694 0.6393 0.0552 0.118 Uiso 1 1 calc R . .
C12 C 0.2081(3) -0.1012(3) -0.1142(3) 0.0918(10) Uani 1 1 d . . .
H12 H 0.2003 -0.1594 -0.1620 0.110 Uiso 1 1 calc R . .
C13 C 0.1506(3) -0.0216(3) -0.1177(3) 0.1000(11) Uani 1 1 d . . .
H13 H 0.1028 -0.0258 -0.1677 0.120 Uiso 1 1 calc R . .
C18 C 0.4869(3) 0.3600(4) 0.3559(3) 0.0986(12) Uani 1 1 d . . .
H18 H 0.4992 0.4076 0.4155 0.118 Uiso 1 1 calc R . .
C3 C -0.0645(2) 0.2798(3) 0.3738(3) 0.1001(11) Uani 1 1 d . . .
H3 H -0.0958 0.2618 0.4389 0.120 Uiso 1 1 calc R . .
C4 C -0.0883(2) 0.3640(3) 0.3089(4) 0.0975(11) Uani 1 1 d . . .
H4 H -0.1358 0.4035 0.3295 0.117 Uiso 1 1 calc R . .
C19 C 0.5371(3) 0.2736(4) 0.3448(4) 0.1108(14) Uani 1 1 d . . .
H19 H 0.5837 0.2624 0.3956 0.133 Uiso 1 1 calc R . .
C25 C 0.2901(3) 0.5984(3) -0.1135(3) 0.0953(10) Uani 1 1 d . . .
H25A H 0.2598 0.5580 -0.1732 0.114 Uiso 1 1 calc R . .
H25B H 0.2928 0.6704 -0.1399 0.114 Uiso 1 1 calc R . .


_geom_special_details            
;
 All esds (except the esd in the dihedral angle between two l.s. planes) 
 are estimated using the full covariance matrix.  The cell esds are taken 
 into account individually in the estimation of esds in distances, angles 
 and torsion angles; correlations between esds in cell parameters are only 
 used when they are defined by crystal symmetry.  An approximate (isotropic) 
 treatment of cell esds is used for estimating esds involving l.s. planes. 
;
loop_
_geom_bond_atom_site_label_1
_geom_bond_atom_site_label_2
_geom_bond_distance
_geom_bond_site_symmetry_2
_geom_bond_publ_flag
O2 C7 1.334(3) . ?
O2 C8 1.448(3) . ?
C7 O1 1.198(3) . ?
C7 C1 1.473(4) . ?
N1 C15 1.449(3) . ?
N1 C22 1.475(3) . ?
N1 C16 1.407(3) . ?
C1 C6 1.376(4) . ?
C1 C2 1.376(4) . ?
C15 H15A 0.9700 . ?
C15 H15B 0.9700 . ?
C15 C8 1.518(3) . ?
C27 H27A 0.9700 . ?
C27 H27B 0.9700 . ?
C27 C22 1.510(3) . ?
C27 C26 1.508(4) . ?
C8 H8 0.9800 . ?
C8 C9 1.499(4) . ?
C22 H22 0.9800 . ?
C22 C23 1.509(4) . ?
C9 C14 1.369(4) . ?
C9 C10 1.371(4) . ?
C16 C17 1.395(4) . ?
C16 C21 1.379(4) . ?
C6 H6 0.9300 . ?
C6 C5 1.376(4) . ?
C23 H23A 0.9700 . ?
C23 H23B 0.9700 . ?
C23 C24 1.531(5) . ?
C26 H26A 0.9700 . ?
C26 H26B 0.9700 . ?
C26 C25 1.485(5) . ?
C17 H17 0.9300 . ?
C17 C18 1.370(5) . ?
C21 H21 0.9300 . ?
C21 C20 1.395(5) . ?
C14 H14 0.9300 . ?
C14 C13 1.380(4) . ?
C2 H2 0.9300 . ?
C2 C3 1.374(5) . ?
C10 H10 0.9300 . ?
C10 C11 1.377(4) . ?
C5 H5 0.9300 . ?
C5 C4 1.365(5) . ?
C11 H11 0.9300 . ?
C11 C12 1.347(5) . ?
C20 H20 0.9300 . ?
C20 C19 1.350(6) . ?
C24 H24A 0.9700 . ?
C24 H24B 0.9700 . ?
C24 C25 1.500(5) . ?
C12 H12 0.9300 . ?
C12 C13 1.354(5) . ?
C13 H13 0.9300 . ?
C18 H18 0.9300 . ?
C18 C19 1.360(6) . ?
C3 H3 0.9300 . ?
C3 C4 1.354(5) . ?
C4 H4 0.9300 . ?
C19 H19 0.9300 . ?
C25 H25A 0.9700 . ?
C25 H25B 0.9700 . ?

loop_
_geom_angle_atom_site_label_1
_geom_angle_atom_site_label_2
_geom_angle_atom_site_label_3
_geom_angle
_geom_angle_site_symmetry_1
_geom_angle_site_symmetry_3
_geom_angle_publ_flag
C7 O2 C8 117.14(19) . . ?
O2 C7 C1 112.3(2) . . ?
O1 C7 O2 122.8(2) . . ?
O1 C7 C1 124.9(2) . . ?
C15 N1 C22 115.37(18) . . ?
C16 N1 C15 118.0(2) . . ?
C16 N1 C22 115.9(2) . . ?
C6 C1 C7 122.4(2) . . ?
C6 C1 C2 119.3(3) . . ?
C2 C1 C7 118.2(3) . . ?
N1 C15 H15A 109.2 . . ?
N1 C15 H15B 109.2 . . ?
N1 C15 C8 111.84(19) . . ?
H15A C15 H15B 107.9 . . ?
C8 C15 H15A 109.2 . . ?
C8 C15 H15B 109.2 . . ?
H27A C27 H27B 108.0 . . ?
C22 C27 H27A 109.3 . . ?
C22 C27 H27B 109.3 . . ?
C26 C27 H27A 109.3 . . ?
C26 C27 H27B 109.3 . . ?
C26 C27 C22 111.6(2) . . ?
O2 C8 C15 104.80(19) . . ?
O2 C8 H8 109.6 . . ?
O2 C8 C9 111.1(2) . . ?
C15 C8 H8 109.6 . . ?
C9 C8 C15 111.97(19) . . ?
C9 C8 H8 109.6 . . ?
N1 C22 C27 112.9(2) . . ?
N1 C22 H22 106.7 . . ?
N1 C22 C23 112.6(2) . . ?
C27 C22 H22 106.7 . . ?
C23 C22 C27 110.9(2) . . ?
C23 C22 H22 106.7 . . ?
C14 C9 C8 122.3(2) . . ?
C14 C9 C10 118.1(3) . . ?
C10 C9 C8 119.5(2) . . ?
C17 C16 N1 119.2(3) . . ?
C21 C16 N1 123.4(3) . . ?
C21 C16 C17 117.4(3) . . ?
C1 C6 H6 120.1 . . ?
C1 C6 C5 119.9(3) . . ?
C5 C6 H6 120.1 . . ?
C22 C23 H23A 109.6 . . ?
C22 C23 H23B 109.6 . . ?
C22 C23 C24 110.1(3) . . ?
H23A C23 H23B 108.1 . . ?
C24 C23 H23A 109.6 . . ?
C24 C23 H23B 109.6 . . ?
C27 C26 H26A 109.5 . . ?
C27 C26 H26B 109.5 . . ?
H26A C26 H26B 108.1 . . ?
C25 C26 C27 110.7(3) . . ?
C25 C26 H26A 109.5 . . ?
C25 C26 H26B 109.5 . . ?
C16 C17 H17 119.6 . . ?
C18 C17 C16 120.8(4) . . ?
C18 C17 H17 119.6 . . ?
C16 C21 H21 119.8 . . ?
C16 C21 C20 120.3(3) . . ?
C20 C21 H21 119.8 . . ?
C9 C14 H14 119.8 . . ?
C9 C14 C13 120.4(3) . . ?
C13 C14 H14 119.8 . . ?
C1 C2 H2 120.0 . . ?
C3 C2 C1 119.9(3) . . ?
C3 C2 H2 120.0 . . ?
C9 C10 H10 119.7 . . ?
C9 C10 C11 120.6(3) . . ?
C11 C10 H10 119.7 . . ?
C6 C5 H5 119.8 . . ?
C4 C5 C6 120.3(3) . . ?
C4 C5 H5 119.8 . . ?
C10 C11 H11 119.5 . . ?
C12 C11 C10 121.0(3) . . ?
C12 C11 H11 119.5 . . ?
C21 C20 H20 119.4 . . ?
C19 C20 C21 121.2(4) . . ?
C19 C20 H20 119.4 . . ?
C23 C24 H24A 109.2 . . ?
C23 C24 H24B 109.2 . . ?
H24A C24 H24B 107.9 . . ?
C25 C24 C23 112.1(3) . . ?
C25 C24 H24A 109.2 . . ?
C25 C24 H24B 109.2 . . ?
C11 C12 H12 120.5 . . ?
C11 C12 C13 119.0(3) . . ?
C13 C12 H12 120.5 . . ?
C14 C13 H13 119.5 . . ?
C12 C13 C14 120.9(3) . . ?
C12 C13 H13 119.5 . . ?
C17 C18 H18 119.4 . . ?
C19 C18 C17 121.3(4) . . ?
C19 C18 H18 119.4 . . ?
C2 C3 H3 119.7 . . ?
C4 C3 C2 120.6(3) . . ?
C4 C3 H3 119.7 . . ?
C5 C4 H4 120.0 . . ?
C3 C4 C5 120.0(3) . . ?
C3 C4 H4 120.0 . . ?
C20 C19 C18 119.0(4) . . ?
C20 C19 H19 120.5 . . ?
C18 C19 H19 120.5 . . ?
C26 C25 C24 110.7(3) . . ?
C26 C25 H25A 109.5 . . ?
C26 C25 H25B 109.5 . . ?
C24 C25 H25A 109.5 . . ?
C24 C25 H25B 109.5 . . ?
H25A C25 H25B 108.1 . . ?

