戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 28304作成日:2026年10月25日

1,3-Propanediol → 1-(z,z,z,z,z,z-Docosa-4,7,10,13,16,19-hexaenoyloxy)-3-hydroxypropane

https://huagongshe.com/reaction/28304

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DicyclohexylcarbodiimideHCID 10868—
反応物DoconexentHCID 445580—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物1-(z,z,z,z,z,z-Docosa-4,7,10,13,16,19-hexaenoyloxy)-3-hydroxypropaneHCID 86758951—

反応手順

A solution of z,z,z,z,z,z-docosa-4,7,10,13,16,19-hexaenoic acid (6.4 g, 19.5 mmol) in methylene chloride (225 ml) was added dropwise to a solution of 1,3-propane diol (7.5 g, 99 mmol), 1,3-dicyclohexylcarbodiimide (4.65 g, 20 mmol) and 4-(N,N-dimethylamino)pyridine (2.1 g, 17 mmol) in methylene chloride (225 ml) at −10° C. The reaction mixture was stirred overnight, warming up to room temperature. The reaction was filtered, concentrated and purified by flash chromatography (ethyl acetate/hexane) to yield 1-(z,z,z,z,z,z-docosa-4,7,10,13,16,19-hexaenoyloxy)-3-hydroxypropane as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE040480E1
出典データセットuspto-grants-2008_09
ORD IDord-ba77b7c555334b5fb024de271e85041c
出典メモuspto-grants-2008_09