Sodium hydride → HCID 23081356、化合物
反応式
[I-].[CH3:2][S+](C)(C)=O.[H-].[Na+].[F:9][C:10]([F:25])([F:24])[C:11]1[CH:16]=[CH:15][C:14]([N:17]2[CH2:22][CH2:21][C:20](=[O:23])[CH2:19][CH2:18]2)=[CH:13][CH:12]=1>CS(C)=O>[F:25][C:10]([F:9])([F:24])[C:11]1[CH:12]=[CH:13][C:14]([N:17]2[CH2:22][CH2:21][C:20]3([O:23][CH2:2]3)[CH2:19][CH2:18]2)=[CH:15][CH:16]=1参加物
5
実験手順
Trimethylsulfoxonium iodide (2.00 g, 9.02 mmol) was gradually added to a suspension of sodium hydride (361 mg, 9.02 mmol) in dimethylsulfoxide (30 ml), and the mixture was stirred at room temperature for 1 hour. To which a solution of 1-(4-trifluoromethylphenyl)piperidin-4-one (2.00 g, 8.2 mmol) in DMSO (10 ml) was added, and the mixture was stirred overnight. The reaction mixture was poured into ice water, and extracted with diethyl ether. The extract was washed with brine, dried over sodium sulfate, and then filtered. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=5/1) to afford 6-(4-trifluoromethylphenyl)-1-oxa-6-azaspiro[2,5]octane (1.51 g, yield 72%) as a pale yellow crystalline powder.