참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Heptanoic Acid | HCID 8094 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-one | HCID 15593764 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 16beta-Ethyl-17beta-n-heptanoyloxyacetoxy-4-estren-3-one | HCID 70467646 | 64% |
반응 단계
In 30 ml of acetone is dissolved 2.6 g of n-heptanoic acid, and 10 ml of 2N-NaOH, 4.2 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one, 30 ml of DMF and 10 ml of water are serially added to the above solution. The mixture is refluxed for 5 hours. After cooling, 400 ml of ethyl acetate is added and the mixture is washed with water and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following 400 ml of diisopropyl ether-n-hexane (2:3), elution is carried out with 1000 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 3.0 g of the above-identified compound as a light-yellow viscous oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04609650 |
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| 출처 데이터셋 | uspto-grants-1986_09 |
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| ORD ID | ord-51711f58cf9043d294756a7ccce7d9b7 |
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| 출처 메모 | uspto-grants-1986_09 |
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