3-Cyanopyridine → 2,4-difluoro-N-(pyridin-3-ylmethyl)aniline

HRID 1656113노트

반응식

HRID 1656113 반응식
[C:1]([C:3]1[CH:4]=[N:5][CH:6]=[CH:7][CH:8]=1)#[N:2].[F:9][C:10]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:11]=1N.[H][H]>[Rh]>[F:9][C:10]1[CH:16]=[C:15]([F:17])[CH:14]=[CH:13][C:11]=1[NH:2][CH2:1][C:3]1[CH:4]=[N:5][CH:6]=[CH:7][CH:8]=1

참가 물질

5

반응물 3

HCID 793-CyanopyridineHCID 97092,4-DifluoroanilineHCID 178418361HCID 178418361, 화합물3회

생성물 1

HCID 110961292,4-difluoro-N-(pyridin-3-ylmethyl)aniline

시약·촉매·용매 1

HCID 23948Rhodium촉매

실험 절차

A mixture of 3-cyanopyridine (10.4 g), 2,4-difluoroaniline (129.1 g) and a 5% rhodium on carbon catalyst (1.0 g) was treated with hydrogen at 60 psig and 25-30 deg C. until two equivalents of hydrogen had reacted. The hydrogen pressure was incrementally increased to 400 psig during the course of the reaction. After cooling, venting and purging with nitrogen, the catalyst was removed by filtration. The filtrate analyzed and found to contain 10.4 g of N-(2,4-diflourophenyl)-N-(3-pyridylmethyl)amine which could be isolated by distillation (158-164 deg. C. @ 3mm Hg) and recrystallization (cyclohexane) to give a white solid with a melting point of 88.5-90 deg C.

후처리

  1. temperatureAfter cooling
  2. custompurging with nitrogen
  3. customthe catalyst was removed by filtration
  4. customcould be isolated by distillation (158-164 deg. C. @ 3mm Hg) and recrystallization (cyclohexane)
  5. customto give a white solid with a melting point of 88.5-90 deg C

출처 및 근거

ORD 기록
ord-25aecfd4b0c34e67882dfb765440ee9f
출처 데이터셋
uspto-grants-1993_10
특허 번호
US05252741

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