Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 4-Dodecanoxy-2-triethylsilylfuran
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 1-Iodododecane | HCID 20282 | — |
| 반응물 | Potassium hydride | HCID 82127 | — |
| 반응물 | 4-Hydroxymethyl-2-triethylsilylfuran | HCID 15037035 | — |
| 생성물 | 4-Dodecanoxy-2-triethylsilylfuran | HCID 19019857 | — |
반응 단계
A solution of 4-hydroxymethyl-2-triethylsilylfuran (Compound 1, 160 mg, 0.75 mmol) in tetrahydrofuran (0.5 ml) was added to a suspension of potassium hydride (33 mg, 0.83 mmol) in tetrahydrofuran (1 ml) at room temperature. When all the potassium hydride disappeared, 1-iodododecane (0.37 ml, 1.5 mmol) was added. Stirring was continued for 4 days at room temperature. The reaction mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 5% ethyl ether/hexane. Fractions with Rf of about 0.65 on evaporation gave the titled ether as a pale yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05298633 |
| 출처 데이터셋 | uspto-grants-1994_03 |
| ORD ID | ord-413aef5246c04bbdab4f6f30a2fe0bdb |
| 출처 메모 | uspto-grants-1994_03 |