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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-(Benzyl-methyl-amino)-1-(4-fluorophenyl)-ethanol → 1-(4-Fluorophenyl)-2-(methylamino)ethan-1-ol

HRID 1351254
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HRID 1351254 반응식
[CH2:1]([N:8](C)[CH2:9][CH:10]([C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=1)[OH:11])C1C=CC=CC=1>C(OCC)(=O)C.CO.[C].[Pd]>[F:18][C:15]1[CH:14]=[CH:13][C:12]([CH:10]([OH:11])[CH2:9][NH:8][CH3:1])=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 216560842-(Benzyl-methyl-amino)-1-(4-fluorophenyl)-ethanol

생성물 1

HCID 219434071-(4-Fluorophenyl)-2-(methylamino)ethan-1-ol수율 72.4%

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 21584119Ethylacetate methanol용매

실험 절차

2-(Benzyl-methyl-amino)-1-(4-fluorophenyl)-ethanol (54.6 g) and 10% palladium-carbon (5.8 g) was stirred in ethyl acetate-methanol (3:1) (800 mL) at 50° C. under hydrogen atmosphere for three hours. The catalyst was removed by filtration, and the filtrate was concentrated. After solidifying with an ether-hexane solvent, and the title compound (25.8 g) was obtained as a colorless solid.

후처리

  1. customThe catalyst was removed by filtration
  2. concentrationthe filtrate was concentrated

출처 및 근거

ORD 기록
ord-d3c946016f154fe79a591d04e117764f
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07217723B2

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