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HRID 1781998作成日:2026年10月24日

Dimethyl Sulfoxide → Benzyl 4-methylidenepiperidine-1-carboxylate

https://huagongshe.com/ja/reaction/1781998

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
生成物Benzyl 4-methylidenepiperidine-1-carboxylateHCID 15519136—

反応条件

温度60 °C

反応手順

A sodium hydride (13.2 g) was added to an anhydrous dimethylsulfoxide (176 mL) and the mixture was heated for 2 hours at 60° C. After cooling, to a suspension of methyltriphenylphosphonium bromide (110.4 g) in dimethylsulfoxide (120 mL) was added the reaction mixture, and the mixture was stirred for 30 minutes at room temperature. To the reaction mixture was added a solution of benzyl 4-oxo-1-piperidinecarboxylate (60 g) in dimethylsulfoxide (150 mL), the mixture was stirred for 1 hour at 50° C. After cooling, to the mixture was added water (2.5 L) and the mixture was extracted with ethyl acetate (1.5 L). The organic layer was washed with a saturated aqueous solution of ammonium chloride (0.5 L) and a saturated aqueous solution of sodium chloride (0.5 L), dried and then concentrated. The obtained residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate:chloroform=9:1:1) to give the title compound (51.1 g) having the following physical data.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07498323B2
出典データセットuspto-grants-2009_03
ORD IDord-976196165fb343849eb72f934f0676e2
出典メモuspto-grants-2009_03