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Acetamide, N-(2-methyl-4-nitrophenyl)- → 4'-Amino-2'-methylacetanilide

HRID 436544
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HRID 436544 반응식
[NH:1]([C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-])=O)=[CH:7][C:6]=1[CH3:14])[C:2]([CH3:4])=[O:3].[H][H]>[Ni].CN(C)C=O>[NH:1]([C:5]1[CH:10]=[CH:9][C:8]([NH2:11])=[CH:7][C:6]=1[CH3:14])[C:2]([CH3:4])=[O:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 75936Acetamide, N-(2-methyl-4-nitrophenyl)-HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 3143384'-Amino-2'-methylacetanilide

시약·촉매·용매 2

HCID 935Nickel촉매HCID 6228Dimethylformamide용매

실험 절차

19.4g (0.1 mole) of 4-acetamino-3-methyl-nitrobenzene, 30g of dimethylformamide and 1g of fresh-developed Raney nickel were fed in an autoclave, 50kg/cm2 of hydrogen was then fed thereto, and, after the reaction was carried out at 60° to 120° C while stirring, the reaction mixture was removed immediately, the Raney nickel was removed while hot, and thereafter the product was poured into 100ml of methanol to separate the 4-acetamino-3-methylaniline produced.

후처리

  1. customwas carried out at 60° to 120° C
  2. customthe reaction mixture was removed immediately
  3. customthe Raney nickel was removed while hot, and thereafter the product
  4. additionwas poured into 100ml of methanol
  5. customto separate the 4-acetamino-3-methylaniline
  6. customproduced

출처 및 근거

ORD 기록
ord-1170cedb5a914ef7a9703441e9dbd141
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04009205

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