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Sodium → 4-Chloro-6-fluoro-2-methoxy-3-nitrophenylamine

HRID 394441
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HRID 394441 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([NH:9]C(=O)C)=[C:4]([O:13][CH3:14])[C:3]=1[N+:15]([O-:17])=[O:16].[Na]>Cl>[Cl:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([NH2:9])=[C:4]([O:13][CH3:14])[C:3]=1[N+:15]([O-:17])=[O:16]
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참가 물질

4

반응물 2

HCID 5360545SodiumHCID 18176014N-(4-chloro-6-fluoro-2-methoxy-3-nitrophenyl)acetamide

생성물 1

HCID 181760194-Chloro-6-fluoro-2-methoxy-3-nitrophenylamine

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

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온도
20 °C

실험 절차

A suspension of 40.0 g (152 mmol) of N-(4-chloro-6-fluoro-2-methoxy-3-nitrophenyl)acetamide in 800 ml of 6M hydrochloric acid was heated for 5 hours at reflux temperature, whereupon the mixture was stirred overnight at approximately 20° C. For work-up, the reaction mixture was stirred into ice-water. The pH was brought to 8-9 by adding sodium solution. The mixture was subsequently extracted six times with ethyl acetate. The combined organic phases were dried over magnesium sulfate and then concentrated under reduced pressure. Yield: 33 g (98%);

후처리

  1. temperaturewas heated for 5 hours
  2. temperatureat reflux temperature
  3. extractionThe mixture was subsequently extracted six times with ethyl acetate
  4. dry with materialThe combined organic phases were dried over magnesium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-035b001e45484f1e8bfe8129ab85ad10
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06602825B1

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