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Methanol → 5-(Trifluoromethyl)-3-thiophenemethanol

HRID 2203012
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인쇄 미리보기

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HRID 2203012 반응식
[F:1][C:2]([F:13])([F:12])[C:3]1[S:7][CH:6]=[C:5]([C:8](OC)=[O:9])[CH:4]=1.CO.[BH4-].[Na+]>C1COCC1>[F:12][C:2]([F:1])([F:13])[C:3]1[S:7][CH:6]=[C:5]([CH2:8][OH:9])[CH:4]=1
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참가 물질

5

반응물 3

HCID 887MethanolHCID 4311764Sodium borohydrideHCID 89690311Methyl 5-(trifluoromethyl)thiophene-3-carboxylate

생성물 1

HCID 199573935-(Trifluoromethyl)-3-thiophenemethanol수율 99.1%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

To a solution of methyl 5-(trifluoromethyl)thiophene-3-carboxylate (523 mg) in THF (1 ml)-MeOH (1 ml) was added NaBH4 (2.2 g) at room temperature, and the reaction mixture was stirred at 60° C. for 3 h. The reaction mixture was quenched with water, and extracted with EtOAc. The extract was washed with brine, dried over MgSO4, concentrated and purified by silica gel column chromatography (hexane/EtOAc) to give the title compound (449 mg) as a pale yellow oil.

후처리

  1. customThe reaction mixture was quenched with water
  2. extractionextracted with EtOAc
  3. washThe extract was washed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. custompurified by silica gel column chromatography (hexane/EtOAc)

출처 및 근거

ORD 기록
ord-1e2c80422bdb4179887d3c9cdb8d9899
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365540B2

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