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HRID 1112作成日:2026年10月25日

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

https://huagongshe.com/reaction/1112

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物NitrogenHCID 947—
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物15-(2-Tetrahydropyranyloxy)pentadecanalHCID 19694657—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-Tetrahydropyranyloxy)-15-hexadeceneHCID 1105643646%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723497
出典データセットuspto-grants-1998_03
ORD IDord-9575b1a855c84db398427cd5e89360d1
出典メモuspto-grants-1998_03