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Methyl 1-(4-hydroxy-3-nitrophenyl)cyclopropanecarboxylate → 1-(3-Amino-4-hydroxy-phenyl)-cyclopropanecarboxylic acid methyl ester

HRID 39134
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HRID 39134 반응식
[CH3:1][O:2][C:3]([C:5]1([C:8]2[CH:13]=[CH:12][C:11]([OH:14])=[C:10]([N+:15]([O-])=O)[CH:9]=2)[CH2:7][CH2:6]1)=[O:4]>CO.[Ni]>[CH3:1][O:2][C:3]([C:5]1([C:8]2[CH:13]=[CH:12][C:11]([OH:14])=[C:10]([NH2:15])[CH:9]=2)[CH2:7][CH2:6]1)=[O:4]
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참가 물질

4

반응물 1

HCID 59129293Methyl 1-(4-hydroxy-3-nitrophenyl)cyclopropanecarboxylate

생성물 1

HCID 591293241-(3-Amino-4-hydroxy-phenyl)-cyclopropanecarboxylic acid methyl ester수율 74%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

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온도
35 °C

실험 절차

To a solution of 1-(4-hydroxy-3-nitro-phenyl)-cyclopropanecarboxylic acid methyl ester (8.3 g, 35.0 mmol) in MeOH (100 mL) was added Raney Ni (0.8 g) under nitrogen atmosphere. The mixture was stirred under hydrogen atmosphere (1 atm) at 35° C. for 8 hours. The catalyst was filtered off through a Celite pad and the filtrate was evaporated under vacuum to give crude product, which was purified by column chromatography on silica gel (P.E./EtOAc 1:1) to give 1-(3-amino-4-hydroxy-phenyl)-cyclopropanecarboxylic acid methyl ester (5.3 g, 74%). 1H NMR (CDCl3, 400 MHz) δ 6.77 (s, 1H), 6.64 (d, J=2.0 Hz, 2H), 3.64 (s, 3H), 1.55-1.52 (m, 2H), 1.15-1.12 (m, 2H).

후처리

  1. filtrationThe catalyst was filtered off through a Celite pad
  2. customthe filtrate was evaporated under vacuum
  3. customto give crude product, which
  4. customwas purified by column chromatography on silica gel (P.E./EtOAc 1:1)

출처 및 근거

ORD 기록
ord-23d9f10b03764aad91d61c9c2215d667
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524767B2

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