Ammonia → 2-Amino-2-(4-chloro-3-fluorophenyl)acetonitrile

HRID 384871노트

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HRID 384871 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][C:3]=1[F:10].[NH3:11].C[Si]([C:16]#[N:17])(C)C.O>CO.CC([O-])C.CC([O-])C.CC([O-])C.CC([O-])C.[Ti+4]>[NH2:11][CH:6]([C:5]1[CH:8]=[CH:9][C:2]([Cl:1])=[C:3]([F:10])[CH:4]=1)[C:16]#[N:17]

참가 물질

7

실험 절차

To a solution of 25.0 g (158 mmol) 4-chloro-3-fluorobenzaldehyde in 130 ml methanol and 175 ml methanol saturated with ammonia were added 54.9 ml (52.7 g, 185 mmol) tetraisopropyl orthotitanate and the mixture stirred at ambient temperature for 1.5 hours. Then 20.35 ml (16.14 g, 163 mmol) trimethylsilyl cyanide were added drop-wise and the resulting mixture stirred at ambient temperature for further 2 hours. The reaction mixture was poured onto 1500 ml iced water and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over Na2SO4 and evaporated. The crude product was purified by flash-chromatography on silica gel with a gradient of heptane and 0 to 50% ethyl acetate. rac-Amino-(4-chloro-3-fluoro-phenyl)-acetonitrile was obtained as orange oil: MS (ISN): 183.2 (M−H)−.

후처리

  1. stirringthe resulting mixture stirred at ambient temperature for further 2 hours
  2. extractionextracted with ethyl acetate
  3. washThe combined organic phases were washed with brine
  4. dry with materialdried over Na2SO4
  5. customevaporated
  6. customThe crude product was purified by flash-chromatography on silica gel with a gradient of heptane and 0 to 50% ethyl acetate

출처 및 근거

ORD 기록
ord-c58137df8a8b447993670e0bde63c0ca
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08367838B2

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