반응식
[CH:1]1([CH2:4][C:5](=O)[CH3:6])[CH2:3][CH2:2]1.[NH3:8].[Cl-].[NH4+:10].[C-:11]#N.[K+]>CCO>[NH2:8][C:5]([CH3:6])([CH2:4][CH:1]1[CH2:3][CH2:2]1)[C:11]#[N:10]참가 물질
실험 절차
To a solution of 1-cyclopropyl-propan-2-one (1.0 g, 10.2 mmol; CAN 4160-75-2) and aqueous ammonia (25% in water, 15 mL) in EtOH (10 mL) was added ammonium chloride (1.63 g, 30.61 mmol). The reaction mixture was stirred at ambient temperature for 1 hour. To this was added potassium cyanide (900 mg, 15.3 mmol) portion wise and the reaction mixture was stirred at ambient temperature for 12 h. Ice water (50 mL) was added and the mixture was extracted with ethyl acetate (3×50 mL). The organic phases were washed with ice water, combined, dried with Na2SO4 and concentrated in vacuo to give the title compound (0.8 g, 63%) as yellow oil. 1H-NMR (DMSO, 400 MHz): 0.14-0.16 (d, 6.4 Hz, 2H); 0.45-0.49 (d, 6.4 Hz, 2H); 0.78-0.85 (m, 1H); 1.39 (s, 3H); 1.46-1.51 (m, 1H), 1.53-1.63 (m, 1H); 2.52 (br s, 2H).
후처리
- stirringthe reaction mixture was stirred at ambient temperature for 12 h
- extractionthe mixture was extracted with ethyl acetate (3×50 mL)
- washThe organic phases were washed with ice water
- dry with materialdried with Na2SO4
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-590bc5693963498ab2930f78b6df8683
- 출처 데이터셋
- uspto-grants-2016_04
- 특허 번호
- US09321727B2
연결된 노트
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