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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Fluoro-4-(4-methoxy-2-trifluoromethyl-phenylamino)-benzonitrile → 2-Fluoro-4-(4-methoxy-2-trifluoromethyl-phenylamino)-benzylamine

HRID 1428203
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인쇄 미리보기

반응식

HRID 1428203 반응식
[F:1][C:2]1[CH:9]=[C:8]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][C:12]=2[C:19]([F:22])([F:21])[F:20])[CH:7]=[CH:6][C:3]=1[C:4]#[N:5]>N.[Ni]>[F:1][C:2]1[CH:9]=[C:8]([NH:10][C:11]2[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][C:12]=2[C:19]([F:20])([F:21])[F:22])[CH:7]=[CH:6][C:3]=1[CH2:4][NH2:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 667656782-Fluoro-4-(4-methoxy-2-trifluoromethyl-phenylamino)-benzonitrile

생성물 1

HCID 667658162-Fluoro-4-(4-methoxy-2-trifluoromethyl-phenylamino)-benzylamine수율 99%

시약·촉매·용매 2

HCID 935Nickel촉매HCID 222Ammonia용매

실험 절차

2-fluoro-4-(4-methoxy-2-trifluoromethyl-phenylamino)-benzonitrile (2.85 g, 9.19 mmol) was hydrogenated in 40 mL saturated methanolic ammonia solution after the addition of 300 mg of Raney nickel at ambient temperature. After the catalyst had been filtered off and the mixture evaporated down the product was obtained in a yield of 99% of theory.

후처리

  1. filtrationAfter the catalyst had been filtered off
  2. customthe mixture evaporated down the product
  3. customwas obtained in a yield of 99% of theory

출처 및 근거

ORD 기록
ord-d714d3e37a9547038799af71c6bf0b43
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08937073B2

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