Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5667생성일: 2026년 10월 23일
Salicylic Acid → 4-Hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile
https://huagongshe.com/ko/reaction/5667
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Salicylic Acid | HCID 338 | — |
| 반응물 | tert-Butyl hydroperoxide | HCID 6410 | — |
| 반응물 | 2-(1-Methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile | HCID 53657145 | — |
| 촉매 | Selenium Dioxide | HCID 24007 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Hydroxy-2-(1-methylethyl)-5,9,13-trimethyl-2,4,8,12-tetradecatetraenenitrile | HCID 86747213 | 317.6% |
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 4-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05245085 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-cd445a28a1bf4a1d9e7cefe6eaf0f6bc |
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| 출처 메모 | uspto-grants-1993_09 |
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