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HRID 537683作成日:2026年10月26日

1,2-Dimethoxyethane → 9-(5-Bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dione

https://huagongshe.com/reaction/537683

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物Iodine, ion (I1+)HCID 3715291—
反応物2-Ethyl-5-bromophenylboronic acidHCID 59445941—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
生成物9-(5-Bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dioneHCID 66679999—

反応条件

温度50 °C

反応手順

A portion of the iodonium ylide (2.0 g, 5.21 mmol) is added to a mixture of 2-ethyl-5-bromophenylboronic acid (1.43 g, 6.25 mmol), palladium(II) acetate (59 mg, 0.26 mmol) and lithium hydroxide monohydrate (0.656 g, 15.6 mmol) in 1,2-dimethoxyethane (40 ml) and water (10 ml), and the mixture is heated at 50° C. for 6 hours, and then allowed to stand at room temperature overnight. The mixture is filtered through diatomaceous earth, washing the filter cake with water (50 ml) and ethyl acetate (50 ml). The organic phase is discarded. The aqueous phase is acidified to pH2 by addition of concentrated hydrochloric acid, and then extracted with ethyl acetate. The organic extract is dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 9-(5-bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dione.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865623B2
出典データセットuspto-grants-2014_10
ORD IDord-145deb73b74741cb952ea9c9df55a26f
出典メモuspto-grants-2014_10