Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → Methyl 6-Fluoro-3,4-dihydro-4-(methoxycarbonyl)-2H-benzopyran-4-butanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Methyl 4-bromobutyrate | HCID 107604 | — |
| 반응물 | Methyl 6-fluorochromane-4-carboxylate | HCID 14986536 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl 6-Fluoro-3,4-dihydro-4-(methoxycarbonyl)-2H-benzopyran-4-butanoate | HCID 19094438 | — |
반응 단계
To a suspension of 8.81 g (0.183 mol) 50% NaH in 300 ml of DMF was added, dropwise, a solution of 27.5 g (0.131 mol) of methyl 6-fluoro-2,3-dihydro-4H-benzopyran-4-carboxylate in 100 ml of DMF. After stirring at room temperature for 1 hour, a solution of 33 g (0.183 mol) of methyl 4-bromobutyrate in 25 ml of DMF was added. The resultant homogeneous solution was stirred at room temperature for 16 hours and then poured onto ice/H2O and acidified to pH 3.0 with concentrated HCl. The aqueous was extracted twice with CH2Cl2 and the combined extracts were dried (NaSO4) and filtered. The filtrate was evaporated in vacuo to an oil (44 g) which was purified by column chromatography on 2 Kg of silica gel, eluting with CH2Cl2 /Et2O.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05294635 |
| 출처 데이터셋 | uspto-grants-1994_03 |
| ORD ID | ord-96d56e5148254c74b3bf53735d2b1973 |
| 출처 메모 | uspto-grants-1994_03 |