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3,5-dinitro-N-(3-nitrophenyl)benzamide → 3,3',5-Triaminobenzanilide

HRID 236992
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인쇄 미리보기

반응식

HRID 236992 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([CH:19]=[C:20]([N+:22]([O-])=O)[CH:21]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-])=O)[CH:11]=1)=[O:8])([O-])=O.[H][H]>[Pd].O1CCOCC1>[NH2:22][C:20]1[CH:19]=[C:6]([CH:5]=[C:4]([NH2:1])[CH:21]=1)[C:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([NH2:16])[CH:11]=1)=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 30945643,5-dinitro-N-(3-nitrophenyl)benzamideHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 213150323,3',5-Triaminobenzanilide

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 312751,4-Dioxane용매

실험 절차

A solution of 13.29 gm. (0.04 mole) of 3,3',5-trinitrobenzanilide in 150 ml. of dioxane is hydrogenated at three atmospheres of hydrogen using 1 gm. of 10% palladium-on-charcoal catalyst. The catalyst is removed by filtration, the filtrate evaporated to dryness under reduced pressure, and the residue dried by distilling 200 ml. of benzene from the reaction mixture.

후처리

  1. customThe catalyst is removed by filtration
  2. customthe filtrate evaporated to dryness under reduced pressure
  3. customthe residue dried
  4. distillationby distilling 200 ml

출처 및 근거

ORD 기록
ord-3459da77b353484cbea9a6dcad6d6396
출처 데이터셋
uspto-grants-1979_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04159341

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