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HCID 21450225, 화합물 → HCID 21450248, 화합물

HRID 596702
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HRID 596702 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:19]=[CH:20][C:21]=1[N+:22]([O-])=O)[C:12]([CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>[OH-].[NH4+]>[NH2:22][C:21]1[CH:20]=[CH:19][C:11]([C:12]([CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[O:13])=[CH:10][C:9]=1[O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 21450225HCID 21450225, 화합물

생성물 1

HCID 21450248HCID 21450248, 화합물

시약·촉매·용매 1

HCID 14923Ammonium Hydroxide용매2회

실험 절차

A solution of 3-(3-benzyloxy-4-nitrobenzoyl)propionic acid in 5N ammonium hydroxide was added to a well stirred boiling aqueous solution of ferrous sulphate. The pH was adjusted to 9 with concentrated ammonium hydroxide and the mixture was refluxed for 15 minutes. The filtrate was concentrated under reduced pressure and then neutralised with glacial acetic acid to give 3-(4-amino-3-benzyloxybenzoyl)propionic acid.

후처리

  1. temperaturethe mixture was refluxed for 15 minutes
  2. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3ccde1d346364bb8906b70a605608ac7
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04011321

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