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Borane → Methyl 2-(4-fluorophenethyl)-5-hydroxymethylbenzoate

HRID 2187627
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반응식

HRID 2187627 반응식
[F:1][C:2]1[CH:22]=[CH:21][C:5]([CH2:6][CH2:7][C:8]2[CH:16]=[CH:15][C:11]([C:12](O)=[O:13])=[CH:10][C:9]=2[C:17]([O:19][CH3:20])=[O:18])=[CH:4][CH:3]=1.O1CCCC1.B>CO>[F:1][C:2]1[CH:22]=[CH:21][C:5]([CH2:6][CH2:7][C:8]2[CH:16]=[CH:15][C:11]([CH2:12][OH:13])=[CH:10][C:9]=2[C:17]([O:19][CH3:20])=[O:18])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6331BoraneHCID 8028Tetrahydrofuran2회HCID 184746364-(4-Fluorophenethyl)-3-methoxycarbonylbenzoic acid

생성물 1

HCID 18474618Methyl 2-(4-fluorophenethyl)-5-hydroxymethylbenzoate수율 82.8%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of 4-(4-fluorophenethyl)-3-methoxycarbonylbenzoic acid (16.5 g, 54.88 mmol), tetrahydrofuran (500 ml) and borane in tetrahydrofuran (1 M. complex, 218 ml, 218 mmol) was stirred under an inert atmosphere at reflux for 6 hours. The reaction was cooled to ambient temperature and methanol (1 L) was added. It was then evaporated to dryness to give a dark oil which was purified by flash chromatography using iso-hexane/ethyl acetate (1:1) as eluant to give as a clear gum methyl 2-(4-fluorophenethyl)-5-hydroxymethylbenzoate (13.10 g).

후처리

  1. temperatureat reflux for 6 hours
  2. customIt was then evaporated to dryness
  3. customto give a dark oil which
  4. customwas purified by flash chromatography

출처 및 근거

ORD 기록
ord-576b3e6a41ee4b9788061b0cc39bc977
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06410539B1

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