Dimethylcarbamoyl Chloride → 4-Chloro-2-pyridinecarbonitrile

HRID 379767

반응식

HRID 379767 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][N+:5]([O-])=[CH:4][CH:3]=1.C[Si]([C:13]#[N:14])(C)C.CN(C)C(Cl)=O.C([O-])([O-])=O.[K+].[K+]>ClCCl>[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([C:13]#[N:14])[CH:3]=1

참가 물질

6

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온도
0 °C

실험 절차

To a mixture of 4-chloropiridine-N-oxide (5.00 g, 38.6 mmol) and trimethylsilyl cyanide (4.84 g, 46.3 mmol) in dichloromethane (60 ml) cooled to 0° C. was added dropwise N,N-dimethylcarbamoyl chloride (3.8 ml, 40.5 mmol). The mixture was allowed to warm to ambient temperature and stirred for 16 h. The mixture was cooled to 0° C. and a 30% aqueous solution of K2CO3 (100 ml) was added. The crude product was extracted with dichloromethane (100 ml×2), the organic extracts dried (MgSO4) and evaporated to give 4-chloro-2-pyridinecarbonitrile (5.35 g, 100%). 1H-NMR (CDCl3) δ: 8.63 (1 H, d, J=4.8 Hz), 7.72 (1 H, d, J=2.6 Hz), 7.55 (1 H, dd, J=1.8, 5.1 Hz).

후처리

  1. temperatureto warm to ambient temperature
  2. temperatureThe mixture was cooled to 0° C.
  3. extractionThe crude product was extracted with dichloromethane (100 ml×2)
  4. dry with materialthe organic extracts dried (MgSO4)
  5. customevaporated

출처 및 근거

ORD 기록
ord-c764c542b61e4969a41983d35d4ac723
출처 데이터셋
uspto-grants-2001_10
특허 번호
US06300363B1

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