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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2'-(Trifluoromethoxy)acetophenone → 1-(2-(Trifluoromethoxy)phenyl)ethanol

HRID 912021
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인쇄 미리보기

반응식

HRID 912021 반응식
[F:1][C:2]([F:14])([F:13])[O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10](=[O:12])[CH3:11].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1.O>[F:1][C:2]([F:13])([F:14])[O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH:10]([OH:12])[CH3:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 27771762'-(Trifluoromethoxy)acetophenoneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 448910731-(2-(Trifluoromethoxy)phenyl)ethanol

시약·촉매·용매 2

HCID 962Water촉매HCID 8028Tetrahydrofuran용매2회

실험 절차

To a solution of 1-(2-Trifluoromethoxyphenyl)ethanone (1.00 g, 4.90 mmol) in THF (5 mL) at 0° C. was added 1M LiAlH4 in THF (5.9 mL, 5.9 mmol), and the solution was allowed to warm to rt. A few drops of water were added to quench. The mixture was concentrated in vacuo, transferred to a separatory funnel, and extracted using DCM and sat. aq. Rochelle salt. The organic layer was concentrated in vacuo to afford the title compound as a clear oil.

후처리

  1. customto quench
  2. concentrationThe mixture was concentrated in vacuo
  3. customtransferred to a separatory funnel
  4. extractionextracted
  5. concentrationThe organic layer was concentrated in vacuo

출처 및 근거

ORD 기록
ord-27d8b26c923143d0abde8c82455186f2
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022206B2

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