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1-(Benzyloxy)-2,3-difluoro-4-nitrobenzene → 4-Amino-2,3-difluorophenol

HRID 520667
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HRID 520667 반응식
C([O:8][C:9]1[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[C:11]([F:18])[C:10]=1[F:19])C1C=CC=CC=1>CO.C1COCC1.[Pd]>[NH2:15][C:12]1[CH:13]=[CH:14][C:9]([OH:8])=[C:10]([F:19])[C:11]=1[F:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 574708771-(Benzyloxy)-2,3-difluoro-4-nitrobenzene

생성물 1

HCID 27787664-Amino-2,3-difluorophenol수율 840.2%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

반응 조건

온도
32 °C

실험 절차

To a suspension of 1-(benzyloxy)-2,3-difluoro-4-nitrobenzene (1.93 g, 0.73 mmol) in CH3OH (45 mL) and THF (9 mL) was added Pd/C (333 mg, 6% Pd content, 53%˜55% water content). The mixture was stirred at 32° C. for 13 hours under H2 atmosphere. The mixture was filtered through a CELITE® pad, which was washed with 50 mL of EtOAc. The filtrate was concentrated in vacuo, washed with 30 mL of CH2Cl2 to give the title compound as a dark brown solid (0.89 g, 84%).

후처리

  1. filtrationThe mixture was filtered through a CELITE® pad, which
  2. washwas washed with 50 mL of EtOAc
  3. concentrationThe filtrate was concentrated in vacuo
  4. washwashed with 30 mL of CH2Cl2

출처 및 근거

ORD 기록
ord-f6d1278c460d4baca81bf9e802fa77d5
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09326975B2

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