Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dodecanoyl chloride → 4-Dodecoyloxymethyl-3-phenyl-2-triethylsilylfuran
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dodecanoyl chloride | HCID 8166 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-Phenyl-2-triethylsilyl-4-furanmethanol | HCID 15037150 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Dodecoyloxymethyl-3-phenyl-2-triethylsilylfuran | HCID 15037151 | — |
반응 단계
To a stirred solution of 3-phenyl-2-triethylsilyl-4-furanmethanol (345 mg, 1.20 mmol) and triethylamine (182 mg, 1.80 mmol) in tetrahydrofuran (15 ml) at 0 degrees under argon was added lauroyl chloride (786 mg, 3.60 mmol). This solution was allowed to warm gradually to room temperature. After stirring an additional 2 hours the white precipitate was filtered off. The filtrate was taken up into ethyl ether, washed with saturated ammonium chloride, saturated sodium bicarbonate, H2O and brine. Evaporation of the dried (magnesium sulfate) extracts gave an oil which was purified by flash chromatography on silica using 2% ethyl ether/hexanes to give the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05298633 |
| 출처 데이터셋 | uspto-grants-1994_03 |
| ORD ID | ord-e4827a66859341669dc5aab13a884a9c |
| 출처 메모 | uspto-grants-1994_03 |