Diethyl (cyanomethyl)phosphonate → Tert-butyl 4-(3-cyanoprop-2-en-1-yl)piperidine-1-carboxylate
반응식
CC(C)([O-])C.[K+].[C:7]([CH2:9]P(=O)(OCC)OCC)#[N:8].O=[CH:19][CH2:20][CH:21]1[CH2:26][CH2:25][N:24]([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH2:23][CH2:22]1>O1CCCC1>[C:7]([CH:9]=[CH:19][CH2:20][CH:21]1[CH2:26][CH2:25][N:24]([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH2:23][CH2:22]1)#[N:8]참가 물질
실험 절차
To a solution of 1.0 M of potassium tert-butoxide in tetrahydrofuran (45.8 mL) at 0° C. was added dropwise a solution of diethyl cyanomethylphosphonate (7.77 mL, 0.0480 mol) in tetrahydrofuran (58.39 mL). The reaction was warmed to room temperature and then cooled at 0° C. again. To the reaction mixture was added a solution of tert-butyl 4-(2-oxoethyl)piperidine-1-carboxylate (9.91 g, 0.0436 mol) in tetrahydrofuran (11.7 mL). The reaction was allowed to warm up to room temperature and stirred at room temperature overnight. After being quenched with water, the mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried and evaporated to dryness. The crude mixture was purified on silica gel, eluting with 0 to 40% EtOAc in hexanes, to give the desired product (8.22 g, 75% in 2 steps). LCMS (M+Na) 273.0.
후처리
- temperaturecooled at 0° C. again
- temperatureto warm up to room temperature
- customAfter being quenched with water
- extractionthe mixture was extracted with EtOAc
- washThe combined organic layers were washed with brine
- customdried
- customevaporated to dryness
- customThe crude mixture was purified on silica gel
- washeluting with 0 to 40% EtOAc in hexanes
출처 및 근거
- ORD 기록
- ord-61f9ed2b28bd4621b70b36aae1e70578
- 출처 데이터셋
- uspto-grants-2012_11
- 특허 번호
- US08309718B2
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