Cyclopropylamine → Ethyl 4-(cyclopropylamino)cyclohexanecarboxylate
반응식
[CH:1]1([NH2:4])[CH2:3][CH2:2]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].O=[C:20]1[CH2:25][CH2:24][CH:23]([C:26]([O:28][CH2:29][CH3:30])=[O:27])[CH2:22][CH2:21]1.C(=O)([O-])O.[Na+]>C(Cl)(Cl)Cl.ClCCCl.C(O)(=O)C>[CH:1]1([NH:4][CH:20]2[CH2:25][CH2:24][CH:23]([C:26]([O:28][CH2:29][CH3:30])=[O:27])[CH2:22][CH2:21]2)[CH2:3][CH2:2]1참가 물질
실험 절차
To a mixture of 3.35 g of cyclopropylamine, 1.0 mL of acetic acid, 9.34 g of sodium triacetoxyborohydride, and 30 mL of 1,2-dichloroethane was added dropwise 5.00 g of ethyl 4-oxocyclohexane carboxylate at room temperature. After stirring at room temperature for 14 hours, to the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution to quench the reaction. To the reaction mixture was added chloroform, followed by extraction and then the organic layer was dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (aqueous ammonia-methanol-chloroform) to obtain 5.62 g of ethyl 4-(cyclopropylamino)cyclohexane carboxylate as a colorless oily substance.
후처리
- customto quench
- customthe reaction
- extractionfollowed by extraction
- dry with materialthe organic layer was dried over anhydrous sodium sulfate
- filtrationAfter filtration
- customthe solvent was evaporated under reduced pressure
- customthe obtained residue was purified by silica gel column chromatography (aqueous ammonia-methanol-chloroform)
출처 및 근거
- ORD 기록
- ord-7fd9576ce5364ebea71ef76111132f1c
- 출처 데이터셋
- uspto-grants-2014_05
- 특허 번호
- US08729068B2
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