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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432972생성일: 2026년 10월 25일

1,3-Propanediol → 1,3-Di-(z,z,z-6,9,12-octadecatrienoyloxy)propane

https://huagongshe.com/reaction/432972

반응식

참여 물질

역할이름HCID투입량
반응물1,3-PropanediolHCID 10442—
반응물Phosphinic AcidHCID 4124402—
반응물Gamma-Linolenic acidHCID 5280933—
생성물1,3-Di-(z,z,z-6,9,12-octadecatrienoyloxy)propaneHCID 86759307—

반응 조건

온도160 °C

반응 단계

z,z,z-6,9,12-Octadecatrienoic acid (available from Sigma Chemicals) (0.180 mol, 50.0 g), propane-1,3-diol (0.086 mol, 6.5 g) and hypophosphorous acid (0.2 g) was heated with stirring to 160° C. under nitrogen. After 6 h, TLC (80:18:2 petroleum ether-ethyl ether-acetic acid) indicated that the reaction had gone to completion (Rf:0.56). The mixture was cooled down to room temperature and petroleum ether (700 mL) was added. The resulting solution was washed with saturated sodium bicarbonate (3×70 mL) and saturated sodium chloride (3×70 mL). It was then dried over anhydrous sodium sulphate and concentrated to dryness. Residual mono-ester and fatty acid were removed by distillation in vacuo (180° C., 10−2 mbar). The resulting oil was dissolved in petroleum ether to make up a 33% solution and was passed down a silica column. Hexane was finally removed to yield 1,3-di-(z,z,z-6,9,12-octadecatrienoyloxy)propane as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664406B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-4966983d9fdf476783aaf4dd3fe37062
출처 메모uspto-grants-2003_12