5-Chloro-2-fluorophenylacetonitrile → Ammonia

HRID 1866535노트

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HRID 1866535 반응식
[BH4-].[Na+].[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([F:13])=[C:8]([CH2:10][C:11]#[N:12])[CH:9]=1>CO.O.O.O.O.O.O.[Co](Cl)Cl>[NH3:12].[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([F:13])=[C:8]([CH2:10][CH2:11][NH2:12])[CH:9]=1

참가 물질

6

실험 절차

Sodium borohydride (1.73 g, 45.51 mmol) was added portionwise to a solution of 5-chloro-2-fluorophenylacetonitrile (1.04 g, 6.15 mmol) and cobalt (II) chloride hexahydrate (2.18 g, 9.22 mmol) in methanol (30 mL) and the mixture was stirred at room temperature for 3 hours. The suspension was then filtered though Celite®, concentrated in vacuo and the residue was partitioned between 1M hydrochloric acid (40 mL) and dichloromethane (40 mL). The aqueous phase was separated, basified to pH 11 with 1M ammonia solution and extracted with dichloromethane (2×40 mL). The combined organic solution was washed with brine (30 mL), dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 98:2:0.2, to afford the title compound as a yellow oil in 33% yield, 350 mg. 1H NMR (400 MHz, CDCl3) δ: 7.28 (1H, m), 7.22 (1H, m), 7.05 (1H, m), 2.85 (2H, m), 2.77 (2H, m) ppm; LRMS APCI m/z 174 [M+H]+

후처리

  1. filtrationThe suspension was then filtered though Celite®
  2. concentrationconcentrated in vacuo
  3. customthe residue was partitioned between 1M hydrochloric acid (40 mL) and dichloromethane (40 mL)
  4. customThe aqueous phase was separated
  5. extractionextracted with dichloromethane (2×40 mL)
  6. washThe combined organic solution was washed with brine (30 mL)
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by column chromatography on silica gel
  10. washeluting with dichloromethane

출처 및 근거

ORD 기록
ord-fa0dd42c78de41339683904186c7b0da
출처 데이터셋
uspto-grants-2009_12
특허 번호
US07629358B2

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