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HRID 1707784作成日:2026年10月26日

Salicylic Acid → 14-Hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile

https://huagongshe.com/reaction/1707784

反応式

関与物質

役割名称HCID仕込み量
反応物Salicylic AcidHCID 338—
反応物tert-Butyl hydroperoxideHCID 6410—
反応物2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 53657145—
触媒Selenium DioxideHCID 24007—
溶媒DichloromethaneHCID 6344—
生成物14-Hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 54348308317.6%

反応手順

To a suspension of selenium dioxide (58 mg) and 2-hydroxybenzoic acid (365 mg) in methylene chloride (10.5 ml) was gradually added an aqueous solution of 80% t-butyl hydroperoxide (11.6 ml) with stirring on a water bath. After 30 minutes, 2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (7.56 g, 26.8 mmol) was added to the mixture, which was then allowed to stand at room temperature for 30 hours. Most of the solvent was removed by evaporation in vacuo, and the residue was dissolved in ether. The organic layer was washed with saturated aqueous sodium bicarbonate, dried over MgSO4, and concentrated. The resultant residue was subjected to silica gel column chromatography to give the aimed 14-hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile (2.53 g, 31%). The starting material was also recovered (3.10 g, 40%) in the column chromatography. The yield of the aimed product based on the consumed starting material was 52%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05354874
出典データセットuspto-grants-1994_10
ORD IDord-c0dc6df34efc4c77bcfc23a67369e20a
出典メモuspto-grants-1994_10