3-Fluorobenzaldehyde → 2,2,2-Trifluoro-1-(3-fluorophenyl)ethan-1-ol

HRID 1186348노트

반응식

HRID 1186348 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[F:10][C:11]([Si](C)(C)C)([F:13])[F:12].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1>[F:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:4]([CH:5]([OH:6])[C:11]([F:13])([F:12])[F:10])[CH:3]=1

참가 물질

5

반응물 3

HCID 680093-FluorobenzaldehydeHCID 552549(Trifluoromethyl)trimethylsilaneHCID 2724141Tetrabutylammonium Fluoride

생성물 1

HCID 232335522,2,2-Trifluoro-1-(3-fluorophenyl)ethan-1-ol수율 120.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

According to Reference Example 8-12, by use of 3-fluorobenzaldehyde (500 mg, 4.03 mmol), (trifluoromethyl)trimethylsilane (715 μL, 4.83 mmol), tetrabutylammonium fluoride (a 1.0 mol/L solution in tetrahydrofuran, 403 μL, 0.403 mmol) and tetrahydrofuran (10 mL), the mixture was stirred and reacted at room temperature for 3 hours. Thus, 1-fluoro-3-(2,2,2-trifluoro-1-hydroxyethyl)benzene (Compound DA) (942 mg, yield: quantitative) was obtained.

후처리

  1. customreacted at room temperature for 3 hours

출처 및 근거

ORD 기록
ord-62e78d7265d94901af7fd8ae80da612e
출처 데이터셋
uspto-grants-2014_03
특허 번호
US08673908B2

반응 노트

불러오는 중…