Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Furan → 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Furan | HCID 8029 | — |
| 반응물 | Acetic acid, 2,2-dichloro-, 1,1'-anhydride | HCID 77772 | — |
| 반응물 | 6-Methoxycarbonyl-1-carboxy-3-hexyne | HCID 10976151 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne | HCID 11020812 | 65% |
반응 단계
A mixture of 6-methoxycarbonyl-1-carboxy-3-hexyne [VI-1] (18.4 g, 0.1 mole), furan (13.6 g, 0.2 mole), dichloroacetic anhydride (28.8 g, 0.12 mole), boron trifluoride ether complex (3.2 g) and toluene (100 ml) is reacted at 20°-30° C. for 10 hours. After completion of the reaction, the reaction mixture is cooled, and washed successively with water, 5% aqueous sodium carbonate solution and water, and the organic layer is dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography to give 1-oxo-1-furyl-7-methoxycarbonyl-4-heptyne [VII-1] (15.2 g, yield; 65%), b.p. 120°-125° C./0.3 mmHg.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05191109 |
| 출처 데이터셋 | uspto-grants-1993_03 |
| ORD ID | ord-8629c017070743739acd5e75fd93c1ef |
| 출처 메모 | uspto-grants-1993_03 |