Methanol → (1R)-1-(2-chlorophenyl)ethan-1-ol

HRID 553699노트

반응식

HRID 553699 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8](=[O:10])[CH3:9].B1(C)OC(C2C=CC=CC=2)(C2C=CC=CC=2)[C@H]2N1CCC2.CSC.B.CO>C1COCC1.O.C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C@H:8]([OH:10])[CH3:9]

참가 물질

8

반응물 4

HCID 887MethanolHCID 72864Ethanone, 1-(2-chlorophenyl)-HCID 2734713(3aS)-1-methyl-3,3-diphenyl-hexahydropyrrolo(1,2-c)(1,3,2)oxazaboroleHCID 12423031(Dimethyl sulfide)trihydroboron

생성물 1

HCID 6999092(1R)-1-(2-chlorophenyl)ethan-1-ol

시약·촉매·용매 3

HCID 962Water용매HCID 6344Dichloromethane용매HCID 8028Tetrahydrofuran용매

실험 절차

2′-Chloroacetophenone (8.4 mL, 65 mmol) and (S)-(−)-2-methyl-CBS-oxazaborolidine (0.90 g, 0.32 mmol) were combined in THF (75 mL). Borane methyl sulfide complex (2M in THF; 21.5 mL, 43 mmol) was added over 20 minutes, and the reaction was stirred at room temperature for 30 minutes. MeOH was added, and the mixture was worked-up with CH2Cl2 and H2O. The organic layer was concentrated to give the title compound.

후처리

  1. concentrationThe organic layer was concentrated

출처 및 근거

ORD 기록
ord-e196a10a0a71453aaaddf8f00d28a16f
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08048902B2

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