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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1707784생성일: 2026년 10월 24일

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

https://huagongshe.com/reaction/1707784

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 was 52%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05354874
출처 데이터셋uspto-grants-1994_10
ORD IDord-c0dc6df34efc4c77bcfc23a67369e20a
출처 메모uspto-grants-1994_10