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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28304생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/28304

반응식

참여 물질

역할이름HCID투입량
반응물1,3-PropanediolHCID 10442—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물DoconexentHCID 445580—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물1-(z,z,z,z,z,z-Docosa-4,7,10,13,16,19-hexaenoyloxy)-3-hydroxypropaneHCID 86758951—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE040480E1
출처 데이터셋uspto-grants-2008_09
ORD IDord-ba77b7c555334b5fb024de271e85041c
출처 메모uspto-grants-2008_09