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HRID 1024493作成日:2026年10月26日

3-Methyl-2-butanone → 1-(3,4-dihydro-2H-1,5-benzodioxepine-7-yl)-4-methyl-1-penten-3-one

https://huagongshe.com/reaction/1024493

反応式

関与物質

役割名称HCID仕込み量
反応物3-Methyl-2-butanoneHCID 11251—
反応物Sodium HydroxideHCID 14798—
反応物3,4-dihydro-2H-1,5-benzodioxepine-7-carbaldehydeHCID 2776388—
溶媒MethanolHCID 887—
生成物1-(3,4-dihydro-2H-1,5-benzodioxepine-7-yl)-4-methyl-1-penten-3-oneHCID 66726288—

反応手順

The MeOH (5 mL) solution of 3,4-dihydro-2H-1,5-benzodioxepine-7-carbaldehyde (445 mg) and 3-methyl-2-butanone (195 mg) was treated with aq. sodium hydroxide (1N, 1 ml) and the mixture was stirred for 24 hours. The reaction was partitioned between 10 ml water and 40 ml ethyl acetate. The organic layer was then sequentially washed with aq. hydrochloric acid (1N, 20 ml), water (20 ml), and Brine (20 ml) and then concentrated under reduced pressure. The residue was purified with flash chromatography on silica (33% ethyl acetate in hexane) to give the desired product as a white crystal.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08722896B2
出典データセットuspto-grants-2014_05
ORD IDord-92691c7ded8f4b29ac0610f63ab42051
出典メモuspto-grants-2014_05