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Hydrazine hydrate (1:1) → Methyl 2-chloro-3-hydrazinocarbonyl-4-methylsulfonylbenzoate

HRID 1276131
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반응식

HRID 1276131 반응식
[Cl:1][C:2]1[C:11]([C:12](Cl)=[O:13])=[C:10]([S:15]([CH3:18])(=[O:17])=[O:16])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].O.[NH2:20][NH2:21]>C(Cl)Cl>[Cl:1][C:2]1[C:11]([C:12]([NH:20][NH2:21])=[O:13])=[C:10]([S:15]([CH3:18])(=[O:17])=[O:16])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 18517408Methyl 2-chloro-3-chlorocarbonyl-4-methylsulfonylbenzoate

생성물 1

HCID 22114944Methyl 2-chloro-3-hydrazinocarbonyl-4-methylsulfonylbenzoate수율 39.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

At room temperature, 3.11 g (10 mmol) of methyl 2-chloro-3-chloroformyl-4-methylsulfonylbenzoate in 50 ml of methylene chloride were added dropwise to 1.0 g (20 mmol) of hydrazine hydrate in 30 ml of methylene chloride. The reaction mixture was stirred at room temperature for 1 hour and then washed with water, dried and concentrated. 1.2 g (39% of theory) of methyl 2-chloro-3-hydrazinocarbonyl-4-methylsulfonylbenzoate were obtained.

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후처리

  1. washwashed with water
  2. customdried
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-989007f211bf4a5591f723e78aacc1b4
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06165944

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