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Ammonia → (4-Aminomethyl-phenyl)-(4-methoxy-2-trifluoromethyl-phenyl)-amine

HRID 1428214
노트
인쇄 미리보기

반응식

HRID 1428214 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10]2[CH:17]=[CH:16][C:13]([C:14]#[N:15])=[CH:12][CH:11]=2)=[C:5]([C:18]([F:21])([F:20])[F:19])[CH:4]=1.N>CO.[Ni]>[NH2:15][CH2:14][C:13]1[CH:12]=[CH:11][C:10]([NH:9][C:6]2[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][C:5]=2[C:18]([F:19])([F:20])[F:21])=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 222AmmoniaHCID 667658264-(4-Methoxy-2-trifluoromethyl-phenylamino)-benzonitrile

생성물 1

HCID 66765571(4-Aminomethyl-phenyl)-(4-methoxy-2-trifluoromethyl-phenyl)-amine

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

3.7 g (12.7 mmol) of 4-(4-methoxy-2-trifluoromethyl-phenylamino)-benzonitrile were hydrogenated in a 7N solution of ammonia in methanol (100 mL) with the addition of Raney nickel at ambient temperature. After the catalyst had been filtered off and the solvent distilled off, the crude product thus obtained was reacted further without purification.

후처리

  1. filtrationAfter the catalyst had been filtered off
  2. distillationthe solvent distilled off

출처 및 근거

ORD 기록
ord-ba359a48b5cd4297b44ae174ad0da289
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08937073B2

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