Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,2,4-Butanetriol → 2,2-Diarachidonyl-4-(2-hydroxyethyl)-[1,3]-dioxolane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,2,4-Butanetriol | HCID 18302 | — |
| 반응물 | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| 반응물 | Diarachidonyl Ketone | HCID 58559565 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2,2-Diarachidonyl-4-(2-hydroxyethyl)-[1,3]-dioxolane | HCID 58559606 | — |
반응 단계
A mixture of diarachidonyl ketone (V, 0.30 g, 0.52 mmol), 1,2,4-butanetriol (0.25 g, 2.4 mmol) and pyridinium p-toluenesulfonate (20 mg) in 60 mL of toluene was refluxed under argon overnight with a Dean-Stark tube to remove water. The resulting mixture was cooled to room temperature. The organic phase was washed with water (2×30 mL), brine (30 mL), and dried over anhydrous Na2SO4. Evaporation of the solvent resulted in a yellowish oily residual. The crude product was purified by column chromatography on silica gel (230-400 mesh, 40 mL) with 0-2% methanol in dichloromethane as eluent. This afforded 0.29 g (84%) of pure VI as pale oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09186325B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-037217f60e9b426c9a4903bbab403f4b |
| 출처 메모 | uspto-grants-2015_11 |