Water → (1R)-1-(2-(Trifluoromethyl)phenyl)ethylamine

HRID 1249888

반응식

HRID 1249888 반응식
[BH4-].[Na+].CO[N:5]=[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[C:14]([F:17])([F:16])[F:15])[CH3:7].O.[OH-].[NH4+]>O1CCCC1.[Cl-].[Cl-].[Cl-].[Cl-].[Zr+4]>[F:15][C:14]([F:16])([F:17])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=1[CH:6]([NH2:5])[CH3:7]

참가 물질

7

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온도
25 °C

실험 절차

Sodium borohydride (1.17 g) is added slowly to a flask containing zirconium tetrachloride (1.8 g) in tetrahydrofuran (27 mL). A solution of 1-(2-trifluoromethyl-phenyl)-ethanone O-methyl-oxime (1.34 g) in tetrahydrofuran (7.7 mL) is added and the resulting solution is stirred at 25° C. for 12 hours. The reaction mixture is then cooled to 0° C. and water (16 mL) is slowly added. Excess ammonium hydroxide is added and the solution is extracted twice with ethyl acetate. The organic portion is washed twice with 1N hydrochloric acid. The aqueous (acid) layer is basified with sodium hydroxide and extracted twice with ethyl acetate. The organic layer is then washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The solvent is removed under reduced pressure to provide the desired product as a yellow oil (0.20 g).

후처리

  1. temperatureThe reaction mixture is then cooled to 0° C.
  2. extractionthe solution is extracted twice with ethyl acetate
  3. washThe organic portion is washed twice with 1N hydrochloric acid
  4. extractionextracted twice with ethyl acetate
  5. washThe organic layer is then washed with saturated aqueous sodium chloride
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customThe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-5c7f23f8364d44d5a25129a2374b3122
출처 데이터셋
uspto-grants-2002_01
특허 번호
US06335350B1

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