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HRID 537683생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/537683

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물Iodine, ion (I1+)HCID 3715291—
반응물2-Ethyl-5-bromophenylboronic acidHCID 59445941—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
생성물9-(5-Bromo-2-ethylphenyl)-3-oxaspiro[5.5]undecane-8,10-dioneHCID 66679999—

반응 조건

온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865623B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-145deb73b74741cb952ea9c9df55a26f
출처 메모uspto-grants-2014_10