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HRID 1112생성일: 2026년 10월 23일

Dimethyl Sulfoxide → 1-(2-Tetrahydropyranyloxy)-15-hexadecene

https://huagongshe.com/ko/reaction/1112

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물NitrogenHCID 947—
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물15-(2-Tetrahydropyranyloxy)pentadecanalHCID 19694657—
촉매Methyltriphenyliphosphonium bromideHCID 74505—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Tetrahydropyranyloxy)-15-hexadeceneHCID 1105643646%

반응 단계

A 300-ml three-necked flask equipped with a stirrer, dropping funnel and N2 inlet tube was charged with 40 ml of dimethyl sulfoxide and 1.2 g (30 mmol) of 60% sodium hydride. The contents were stirred at 75° C. for 1.5 hours in an N2 atmosphere and then cooled to room temperature. To this mixture, a solution of 8.93 g (25 mmol) of methyltriphenylphosphonium bromide in 40 ml of dimethyl sulfoxide was added dropwise over 10 minutes. The resultant mixture was stirred further for 20 minutes at room temperature. To this mixture, a solution of 3.27 g (10 mmol) of 15-(2-tetrahydropyranyloxy)pentadecanal in 15 ml of THF was added dropwise over 5 minutes, followed by stirring further for 30 minutes. After completion of the reaction, the reaction mixture was added with water and subjected to extraction with hexane, followed by concentration under reduced pressure. Thereafter, the resultant residue was purified by flash column chromatography on silica gel, thereby obtaining 1.49 g (yield: 46%) of 1-(2-tetrahydropyranyloxy)-15-hexadecene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723497
출처 데이터셋uspto-grants-1998_03
ORD IDord-9575b1a855c84db398427cd5e89360d1
출처 메모uspto-grants-1998_03