반응 #992714

ord-72056b8dc21f40cba77a26043d527fb4

반응 방정식

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
수율 96.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08012901B1uspto-grants-2011_09