関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Lithium | HCID 3028194 | — |
| 反応物 | 16beta-Ethyl-3-methoxy-1,3,5(10)-estratrien-17beta-ol | HCID 12831647 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | Oxendolone | HCID 443947 | — |
反応手順
A solution of 2.0 g. of 16β-ethyl-3-methoxy-1,3,5(10)-estratrien-17β-ol in 40 ml. of tetrahydrofuran and 4 ml. of tert.-butanol is added dropwise at -40° C. to 80 ml. of ammonia. After the incremental introduction of 1.2 g. of lithium, the mixture is stirred for 2 hours at -40° C.; then the ammonia is allowed to evaporate, the residue is poured into about 200 ml. of water, and the mixture is extracted with ethyl acetate. The crude product is taken up in 40 ml. of methanol and 4 ml. of 4 N hydrochloric acid and agitated for 15 minutes at 50° C. Thereafter, the mixture is poured into water and extracted with methylene chloride. After recrystallizing the crude product from ethyl acetate/ether, 1.7 g. of 16β-ethyl-17β-hydroxy-4-estren-3-one is produced, m.p. 150°-152° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04298538 |
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| 出典データセット | uspto-grants-1981_11 |
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| ORD ID | ord-a7e1eac35c894d3aabd07696fa222da2 |
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| 出典メモ | uspto-grants-1981_11 |
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