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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-Nitrophenoxyacetic acid methyl ester → Methyl 2-(3-aminophenoxy)acetate

HRID 2189019
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반응식

HRID 2189019 반응식
[CH3:1][O:2][C:3](=[O:15])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-])=O)[CH:7]=1>[Pd].CO>[CH3:1][O:2][C:3](=[O:15])[CH2:4][O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([NH2:12])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 107037043-Nitrophenoxyacetic acid methyl ester

생성물 1

HCID 10678961Methyl 2-(3-aminophenoxy)acetate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

Add 1.3 g of palladium on activated carbon (10%) to 13 g (61.6 mmol) of 3-nitrophenoxyacetic acid methyl ester in 150 ml of methanol under argon. Stir the mixture at RT under a hydrogen atmosphere (standard pressure) for 18 h. Filter the catalyst off through kieselguhr and concentrate the filtrate under reduced pressure. After drying under high vacuum, 10.7 g (95.9% of theory) of the target compound are obtained.

후처리

  1. filtrationFilter the catalyst off through kieselguhr
  2. concentrationconcentrate the filtrate under reduced pressure
  3. customAfter drying under high vacuum, 10.7 g (95.9% of theory) of the target compound
  4. customare obtained

출처 및 근거

ORD 기록
ord-d56ddf54de38434db21b0d6402665555
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324222B2

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