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Benzene, 1-nitro-4-[(3-phenylpropyl)thio]- → 4-(3'-Phenyl-propylthio)-aniline

HRID 1415346
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HRID 1415346 반응식
[C:1]1([CH2:7][CH2:8][CH2:9][S:10][C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-])=O)=[CH:13][CH:12]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>[Ni].CN(C)C=O>[C:1]1([CH2:7][CH2:8][CH2:9][S:10][C:11]2[CH:12]=[CH:13][C:14]([NH2:17])=[CH:15][CH:16]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
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참가 물질

4

반응물 1

HCID 11311846Benzene, 1-nitro-4-[(3-phenylpropyl)thio]-

생성물 1

HCID 214818444-(3'-Phenyl-propylthio)-aniline

시약·촉매·용매 2

HCID 935Nickel촉매HCID 6228Dimethylformamide용매

실험 절차

90 g of 4-(3'-phenyl-propylthio)-nitrobenzene is catalytically hydrogenated in 300 ml. of dimethylformamide with Raney nickel. After completion of the hydrogen absorption and removal of the catalyst and the solvent, there is obtained 4-(3'-phenyl-propylthio)-aniline as an oily residue, which can be used without purification in the next reaction stage.

후처리

  1. customAfter completion of the hydrogen absorption and removal of the catalyst

출처 및 근거

ORD 기록
ord-8f76f327261948b3a832277113c2bbc7
출처 데이터셋
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04004907

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