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N-cyclohexyl-2-nitro-4-(trifluoromethyl)aniline → 1-N-cyclohexyl-4-(trifluoromethyl)benzene-1,2-diamine

HRID 1458796
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반응식

HRID 1458796 반응식
[CH:1]1([NH:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][C:9]=2[N+:18]([O-])=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[H][H]>CO.[Pd]>[CH:1]1([NH:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:15])([F:16])[F:17])=[CH:10][C:9]=2[NH2:18])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 3853727N-cyclohexyl-2-nitro-4-(trifluoromethyl)anilineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 24165451-N-cyclohexyl-4-(trifluoromethyl)benzene-1,2-diamine수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

32 g (0.11 mol) of N-cyclohexyl-2-nitro-4-trifluoromethylaniline dissolved in 250 ml of methanol were hydrogenated under a pressure of about 1 bar of hydrogen in the presence of 1.5 g of palladium/active carbon (10% by weight Pd) at room temperature. The reaction mixture was filtered. Conventional workup of the filtrate gave a 100% yield of the abovementioned compound.

후처리

  1. filtrationThe reaction mixture was filtered

출처 및 근거

ORD 기록
ord-7f381552dee249ecb561eac63adc3169
출처 데이터셋
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05852017

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