4-Aminotetrahydro-2H-pyran-4-carboxylic acid hydrochloride → Methyl 4-aminooxane-4-carboxylate
반응식
Cl.[NH2:2][C:3]1([C:9]([OH:11])=[O:10])[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[CH3:12][Si](C=[N+]=[N-])(C)C.C(OCC)C>CO>[NH2:2][C:3]1([C:9]([O:11][CH3:12])=[O:10])[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1참가 물질
4
실험 절차
To a solution of 4-amino-4-carboxy-tetrahydropyrane hydrochloride (2 g) in methanol was added dropwise a solution of 2M trimethylsilyldiazomethane-diethylether (33 mL) under ice-cooling, and the mixture was stirred at room temperature for 4 days. The reaction mixture was concentrated in vacuo, and the resultant crude product was dissolved in hexane-diethylether (1 mL/1 mL), and thereto was added an aqueous 4N hydrochloric acid. The precipitates were collected by filtration to give 4-amino-4-methoxycarbonyl-tetrahydropyrane (2.13 g, yield: 99%) as white-crystals.
후처리
- temperaturecooling
- concentrationThe reaction mixture was concentrated in vacuo
- dissolutionthe resultant crude product was dissolved in hexane-diethylether (1 mL/1 mL)
- additionwas added an aqueous 4N hydrochloric acid
- filtrationThe precipitates were collected by filtration
출처 및 근거
- ORD 기록
- ord-837d8ec3d32d4aaa9b9ad868e3df0f19
- 출처 데이터셋
- uspto-grants-2012_04
- 특허 번호
- US08163759B2
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