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HRID 1023828作成日:2026年10月25日

Methylenecyclohexane → 1-[(4-methylphenyl)sulfonyl]-1-Azaspiro[2.5]octane

https://huagongshe.com/reaction/1023828

反応式

関与物質

役割名称HCID仕込み量
反応物MethylenecyclohexaneHCID 14502—
反応物TosylchloramideHCID 31388—
反応物Phenyltrimethylammonium bromide dibromideHCID 17977687—
溶媒AcetonitrileHCID 6342—
生成物1-[(4-methylphenyl)sulfonyl]-1-Azaspiro[2.5]octaneHCID 1114977248.3%

反応手順

To a stirred suspension of dried Chloramine-T (5.10 g, 20.76 mmol) in CH3CN (100 mL) under a nitrogen atmosphere methylenecyclohexane (9.98 g, 104 mmol) was added. Phenyltrimethylammonium tribromide (7.80 g, 20.76 mmol) was added in three portions over 10 min. The mixture was stirred at room temperature for 16 hours. The solvent was evaporated and the residue was partitioned between dichloromethane and water. The organic layer was dried over Na2SO4 and the solvent was evaporated. The residue was chromatographed on silica gel with an ISCO Combiflash using EtOAc/hexanes (5-30% gradient) to afford the title compound as a white solid (2.66 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722727B2
出典データセットuspto-grants-2014_05
ORD IDord-9d61fe0b5e3049a380a1f5b4ab11c292
出典メモuspto-grants-2014_05