Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl orthoformate → 3-Ethoxy-13-ethylgona-3,5-dien-17-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl orthoformate | HCID 31214 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 13-Ethylgon-4-ene-3,17-dione | HCID 10379264 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 3-Ethoxy-13-ethylgona-3,5-dien-17-one | HCID 69913766 | — |
반응 단계
-Pyridinium p-toluenesulfonate (5.0 g) was added to a solution of 13-ethylgon-4-ene-3,17-dione [Hoffmann-La Roche and Co.; AG, DE 1806410 (1967); 100.0 g] in a mixture of ethanol (600 ml), dioxane (800 ml) and triethyl orthoformate (199 ml). After 4.5 h stirring at room temperature pyridine (100 ml) was added and the reaction mixture was poured into a saturated aqueous solution of sodium hydrogencarbonate. The product was extracted into ethyl acetate; the combined organic phases were washed with water and brine, dried over magnesium sulfate and concentrated under reduced pressure, to give 3-ethoxy-13-ethylgona-3,5-dien-17-one (146.3 g). The product was used in the following step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06541465B2 |
| 출처 데이터셋 | uspto-grants-2003_04 |
| ORD ID | ord-fee1e1af560446e390b5a85ac226eb0d |
| 출처 메모 | uspto-grants-2003_04 |