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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 713845생성일: 2026년 10월 26일

1,2,4-Butanetriol → 2,2-Diarachidonyl-4-(2-hydroxyethyl)-[1,3]-dioxolane

https://huagongshe.com/reaction/713845

반응식

참여 물질

역할이름HCID투입량
반응물1,2,4-ButanetriolHCID 18302—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
반응물Diarachidonyl KetoneHCID 58559565—
용매TolueneHCID 1140—
생성물2,2-Diarachidonyl-4-(2-hydroxyethyl)-[1,3]-dioxolaneHCID 58559606—

반응 단계

A mixture of diarachidonyl ketone (V, 0.30 g, 0.52 mmol), 1,2,4-butanetriol (0.25 g, 2.4 mmol) and pyridinium p-toluenesulfonate (20 mg) in 60 mL of toluene was refluxed under argon overnight with a Dean-Stark tube to remove water. The resulting mixture was cooled to room temperature. The organic phase was washed with water (2×30 mL), brine (30 mL), and dried over anhydrous Na2SO4. Evaporation of the solvent resulted in a yellowish oily residual. The crude product was purified by column chromatography on silica gel (230-400 mesh, 40 mL) with 0-2% methanol in dichloromethane as eluent. This afforded 0.29 g (84%) of pure VI as pale oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09186325B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-037217f60e9b426c9a4903bbab403f4b
출처 메모uspto-grants-2015_11