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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1110175생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1110175

반응식

참여 물질

역할이름HCID투입량
반응물Salicylic AcidHCID 338—
반응물tert-Butyl hydroperoxideHCID 6410—
반응물2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 53657145—
촉매Selenium DioxideHCID 24007—
용매DichloromethaneHCID 6344—
생성물14-Hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrileHCID 54348308317.6%

반응 단계

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 as 52%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05324869
출처 데이터셋uspto-grants-1994_06
ORD IDord-229e6ebae67c49df94db2de2aa9ed455
출처 메모uspto-grants-1994_06