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 | Trifluoroacetic anhydride | HCID 9845 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 6-Methoxycarbonyl-1-carboxy-3-hexyne | HCID 10976151 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne | HCID 11020812 | 92% |
반응 단계
To a mixture of 6-methoxycarbonyl-1-carboxy-3-hexyne [VI-1] (27.6 g, 0.15 mole), furan (30.7 g, 0.45 mole) and dichloromethane (150 ml) is added trifluoroacetic anhydride (37.8 g, 0.18 mole) at room temperature, and the mixture is reacted at 30°-35° C. for 24 hours. After completion of the reaction, the reaction solution is poured into ice-water and neutralized with 20% aqueous sodium hydroxide solution. The organic layer is separated and washed successively with 5% aqueous sodium hydrogen carbonate solution and water. The organic layer is concentrated under reduced pressure to give 1-oxo-1-furyl-7-methoxycarbonyl-4-heptyne [VII-1] (32.3 g, yield; 92%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05191109 |
| 출처 데이터셋 | uspto-grants-1993_03 |
| ORD ID | ord-b61e2a66f6604740a7874d7be8fc8165 |
| 출처 메모 | uspto-grants-1993_03 |