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1-(2-Benzyloxyphenyl)-4-fluoro-3,5-dimethyl-1H-pyrazole → 2-(4-Fluoro-3,5-dimethyl-1H-pyrazol-1-yl)phenol

HRID 337354
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인쇄 미리보기

반응식

HRID 337354 반응식
C([O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[N:15]1[C:19]([CH3:20])=[C:18]([F:21])[C:17]([CH3:22])=[N:16]1)C1C=CC=CC=1>CO.[Pd]>[F:21][C:18]1[C:17]([CH3:22])=[N:16][N:15]([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=2[OH:8])[C:19]=1[CH3:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 867032601-(2-Benzyloxyphenyl)-4-fluoro-3,5-dimethyl-1H-pyrazole

생성물 1

HCID 601440492-(4-Fluoro-3,5-dimethyl-1H-pyrazol-1-yl)phenol수율 100.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

416 mg of 1-(2-benzyloxyphenyl)-4-fluoro-3,5-dimethyl-1H-pyrazol was dissolved in 16 ml of methanol, and 42.6 mg of 10% palladium/carbon was added and stirred under hydrogen atmosphere at room temperature for a whole day and night. After the insoluble matter was filtered off, the filtrate was distilled off under reduced pressure and the resulting residue was purified using silica gel column chromatography (hexane:ethyl acetate=5:1) to yield 290 mg of the title compound.

후처리

  1. filtrationAfter the insoluble matter was filtered off
  2. distillationthe filtrate was distilled off under reduced pressure
  3. customthe resulting residue was purified

출처 및 근거

ORD 기록
ord-7cf7066bbafc45cbbdaccda731848d36
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889727B2

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