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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 3-Nitrophenoxyacetic acid methyl ester

HRID 2189018
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HRID 2189018 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([OH:10])[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].C(=O)([O-])[O-].[Cs+].[Cs+].[CH3:17][O:18][C:19](=[O:22])[CH2:20]Br.O>CC(C)=O>[CH3:17][O:18][C:19](=[O:22])[CH2:20][O:10][C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 10796Cesium carbonateHCID 111373-NitrophenolHCID 60984Methyl bromoacetate

생성물 1

HCID 107037043-Nitrophenoxyacetic acid methyl ester

시약·촉매·용매 1

HCID 180Acetone용매

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온도
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
50 °C

실험 절차

Initially charge 50 g (359.4 mmol) of 3-nitrophenol and 175.67 g (539 mmol) of caesium carbonate in 1.0 liter of acetone and add 71.5 g (467.3 mmol) of bromoacetic acid methyl ester. Stir the mixture at 50° C. for 1 h and, after cooling, pour onto 7.5 liters of water. Stir the suspension for 30 min, then filter off with suction and wash the filter residue with water. Dry the solid in a drying cabinet at 50° C. and 100 mbar. 64.3 g (84.7% of theory) of the target compound are obtained.

후처리

  1. temperatureafter cooling
  2. stirringStir the suspension for 30 min
  3. filtrationfilter off with suction
  4. washwash the filter residue with water
  5. customDry the solid in a drying cabinet at 50° C.
  6. custom64.3 g (84.7% of theory) of the target compound are obtained

출처 및 근거

ORD 기록
ord-1e997f6adffc49e5ac677df267fe6693
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08324222B2

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