戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 432972作成日:2026年10月26日

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

https://huagongshe.com/reaction/432972

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-PropanediolHCID 10442—
反応物Phosphinic AcidHCID 4124402—
反応物Gamma-Linolenic acidHCID 5280933—
生成物1,3-Di-(z,z,z-6,9,12-octadecatrienoyloxy)propaneHCID 86759307—

反応条件

温度160 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664406B1
出典データセットuspto-grants-2003_12
ORD IDord-4966983d9fdf476783aaf4dd3fe37062
出典メモuspto-grants-2003_12