تفاعل #992714

ord-72056b8dc21f40cba77a26043d527fb4

معادلة التفاعل

c1c[nH]cn1
imidazole
O=C(CSc1cccc(O)c1)c1ccc(F)cc1F
9n
O=C(CSc1cccc(O)c1)c1ccc(F)cc1F
1-(2,4-Difluoro-phenyl)-2-(3-hydroxy-phenylsulfanyl)-ethanone
CC(C)[Si](Cl)(C(C)C)C(C)C
TIPSCl
CC(C)[Si](Oc1cccc(SCC(=O)c2ccc(F)cc2F)c1)(C(C)C)C(C)C
1-(2,4-Difluoro-phenyl)-2-(3-triisopropylsilanyloxy-phenylsulfanyl)-ethanone
المردود 96.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe mixture was filtered
  2. 2
    أخرىthe solvents were removed under reduced pressure
  3. 3
    أخرىThe residue was purified by flash column chromatography
  4. 4
    غسيلeluted by hexane:ethyl acetate (6:1)
  5. 5
    أخرىthe correct product was obtained as a slightly yellow oil

الإجراء التجريبي

To a 100 mL three-neck round bottom flask was added 9n (1.4 g, 5 mmol) and TIPSCl (1.15 g, 6 mmol) in CH2Cl2 (40 mL) under nitrogen at room temperature. Then a solution of imidazole (816 mg, 12 mmol) in CH2Cl2 (20 mL) was added dropwise. The resulting mixture was stirred for 24 h. The mixture was filtered and the solvents were removed under reduced pressure. The residue was purified by flash column chromatography eluted by hexane:ethyl acetate (6:1) and the correct product was obtained as a slightly yellow oil; yield 96% (2.1 g); H NMR (400 MHz, CDCl3): d 1.13 (m, 18H, 6×CH3), 1.29 (m, 3H, CH), 4.26 (s, 2H, SCH2), 6.75 (m, 1H, Ar), 6.89-6.97 (m, 4H, Ar), 7.15 (m, 1H, Ar), 7.95 (m, 1H, Ar); CNMR (100 MHz, CDCl3): δ 21.6, 17.7, 29.3, 104.3, 111.5, 118.5, 119.2, 121.5, 122.7, 129.5, 131.4, 135.9, 153.6, 156.3, 159.5, 162.3, 164.9; IR ν (cm−1) 2944, 2983, 2866, 1682, 1610, 1584, 1475, 1423, 1266, 1245, 1186, 1145, 1095, 997, 970, 943, 881, 852, 776, 683; ESI HRMS m/z calcd for C23H31F2O3SSi (M+OH)+ 453.17258, found 453.17226.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08012901B1uspto-grants-2011_09