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Acetyl chloride → N-[3-(4-Methyl-2-nitro-phenylsulfanyl)-phenyl]-acetamide

HRID 2197958
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인쇄 미리보기

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HRID 2197958 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:10]=[C:11]([NH2:15])[CH:12]=[CH:13][CH:14]=2)=[C:4]([N+:16]([O-:18])=[O:17])[CH:3]=1.[C:19](Cl)(=[O:21])[CH3:20]>C(Cl)Cl>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:10]=[C:11]([NH:15][C:19](=[O:21])[CH3:20])[CH:12]=[CH:13][CH:14]=2)=[C:4]([N+:16]([O-:18])=[O:17])[CH:3]=1
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참가 물질

4

반응물 2

HCID 6367Acetyl chlorideHCID 684579173-(4-Methyl-2-nitro-phenylsulfanyl)-phenylamine

생성물 1

HCID 68459008N-[3-(4-Methyl-2-nitro-phenylsulfanyl)-phenyl]-acetamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The title compound was prepared using 3-(4-Methyl-2-nitro-phenylsulfanyl)-phenylamine (8.20 g, 31.50 mmol) and acetyl chloride (2.72 g, 34.65 mmol) dissolved in CH2Cl2. This was stirred at room temperature for 2 hrs at which time the title compound was collected by filtration (8.78 g, 92

후처리

  1. customThe title compound was prepared
  2. filtrationwas collected by filtration (8.78 g, 92

출처 및 근거

ORD 기록
ord-60da73c7dbe445af8b93e8dfc971c12f
출처 데이터셋
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08338605B2

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