Benzeneacetonitrile, 2,3-dichloro- → Ammonia

HRID 1866534노트

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HRID 1866534 반응식
[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9][C:10]#[N:11].[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[Cl-].[Cl-].[Al+3]>C(OCC)C>[NH3:11].[Cl:1][C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][NH2:11]

참가 물질

6

실험 절차

A solution of 2,3-dichlorophenylacetonitrile (0.5 g, 2.7 mmol) in diethyl ether (5 mL) was added to an ice-cold solution of lithium aluminium hydride (1M in diethyl ether, 2.7 mL, 2.7 mmol) and aluminium trichloride (359 mg, 2.7 mmol). The mixture was stirred at room temperature 2.5 hours and was then quenched with 1M sodium hydroxide solution (5 mL). The mixture was stirred for a further 30 minutes and filtered through Celite®. The layers of the filtrate were separated and the organic solution was concentrated in vacuo. Purification of the residue by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 95:5:0.5 afforded the title compound as a clear oil in 26% yield, 135 mg. 1H NMR (400 MHz, CDCl3) δ 7.38 (1H, dd), 7.27-7.19 (2H, m), 2.95 (2H, m), 2.87 (2H, m) ppm; LRMS APCI m/z 190 [M+H]+

후처리

  1. customwas then quenched with 1M sodium hydroxide solution (5 mL)
  2. stirringThe mixture was stirred for a further 30 minutes
  3. filtrationfiltered through Celite®
  4. customThe layers of the filtrate were separated
  5. concentrationthe organic solution was concentrated in vacuo
  6. customPurification of the residue by column chromatography on silica gel
  7. washeluting with dichloromethane

출처 및 근거

ORD 기록
ord-657e9ba6429542548bb9b508f3c155a3
출처 데이터셋
uspto-grants-2009_12
특허 번호
US07629358B2

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