반응식
[CH2:1]([Li])CCC.CCCCCC.[CH3:12][N:13]([CH3:27])[C:14]1([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH2:19][CH2:18][C:17](=[O:20])[CH2:16][CH2:15]1.CI>C1COCC1>[CH3:12][N:13]([CH3:27])[C:14]1([C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH2:19][CH2:18][C:17](=[O:20])[CH:16]([CH3:1])[CH2:15]1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
Diisopropylamine (2.1 ml, 15 mmol) was provided in dry THF in argon and mixed with n-butyl lithium in hexane (2.5M, 6 ml, 15 mmol) at 30° C. The reaction mixture was cooled to −78° C. 4-(dimethylamino)-4-phenylcyclohexanone (2.17 g, 10 mmol), dissolved in 10 ml of dry THF, was added in drops to this solution within 10 min. The batch was stirred for 30 min at −78° C. and then mixed with methyl iodide (1.86 ml, 30 mmol). It was heated to RT and stirred for a further 18 h. The solvent was removed at the rotary evaporator and the residue taken up in DCM. Extraction was conducted with 1N HCl (3×30 ml). The aqueous phase was basified with 5N NaOH (20 ml) and extracted with DCM (3×30 ml). The combined organic phases were washed with H2O (2×10 ml) and dried over Na2SO4. The semisolid residue (1.2 g) obtained after removal of the solvent was recrystallised from ethyl acetate (1 ml).
후처리
- additionwas added in drops to this solution within 10 min
- temperatureIt was heated to RT
- stirringstirred for a further 18 h
- customThe solvent was removed at the rotary evaporator
- extractionExtraction
- extractionextracted with DCM (3×30 ml)
- washThe combined organic phases were washed with H2O (2×10 ml)
- dry with materialdried over Na2SO4
출처 및 근거
- ORD 기록
- ord-0d735cbbb9c2411a9a3f0da231d40022
- 출처 데이터셋
- uspto-grants-2012_10
- 특허 번호
- US08293758B2
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