반응식
[CH:1]1([CH:7]2[CH2:12][CH2:11][CH:10]([C:13]([OH:15])=O)[CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(Cl)(=O)C(Cl)=O.Cl.[CH3:23][NH:24][OH:25]>O1CCCC1.CN(C)C=O.[OH-].[Na+]>[CH:1]1([CH:7]2[CH2:12][CH2:11][CH:10]([C:13]([N:24]([OH:25])[CH3:23])=[O:15])[CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1참가 물질
실험 절차
To a solution of 4-cyclohexyl-cyclohexanecarboxylic acid (1.47 g, 7 mmol) in 50 ml of tetrahydrofuran was added oxalyl chloride (0.67 ml, 7.7 mmol) and a few drops of dimethylformamide. After stirring for one hour, the reaction mixture was concentrated to about 1/3 of the original volume and added dropwise into a cold (~0° C.), stirred solution of N-methylhydroxylamine hydrochloride (1.17 g, 14 mmol) in 40 ml of 1N sodium hydroxide. The mixture was stirred for two hours and extracted three times with ethyl acetate. The combined ethyl acetate extracts were washed twice with water, dried with anhydrous sodium sulfate and concentrated. Purification by flash chromatography and crystallization afforded 0.342 g of 4-cyclohexyl-N-hydroxy-N-methylcyclohexanecarboxamide as a white solid (m.p. 89°-90° C.).
후처리
- concentrationthe reaction mixture was concentrated to about 1/3 of the original volume
- additionadded dropwise into a cold (~0° C.)
- stirringThe mixture was stirred for two hours
- extractionextracted three times with ethyl acetate
- washThe combined ethyl acetate extracts were washed twice with water
- dry with materialdried with anhydrous sodium sulfate
- concentrationconcentrated
- customPurification
- customby flash chromatography and crystallization
출처 및 근거
- ORD 기록
- ord-19b7ee22410040a3bdf1d114a7a46b5d
- 출처 데이터셋
- uspto-grants-1989_12
- 특허 번호
- US04889874
연결된 노트
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