関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanol | HCID 702 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | (3S,8R,9S,10R,13S,14S)-17-iodo-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta(a)phenanthren-3-ol | HCID 11069352 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Androsta-5,16-dien-3 beta-ol | HCID 150900 | — |
反応手順
125 g. of sodium metal were added in small portions to a stirred solution of 21 g. of 3β-hydroxy-17-iodo androsta-5,16-diene in 1.05 l. of anhydrous ethanol. During the addition the mixture was kept at reflux temperature. After all of the sodium was dissolved the reaction mixture was cooled and water was added. The ethanol was removed by distillation under reduced pressure and the resulting aqueous suspension was extracted with methyl isobutyl ketone. The extract was washed until neutral and concentrated to dryness in vacuo. The crystalline residue was recrystallized from methanol-water and 13 g. of 3β-hydroxy-androsta-5,16-diene were obtained. Two crystallizations from acetone yielded the pure compound melting at 137°-138° C. mol. peak in mass spectrum (m/e): 272.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04075233 |
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| 出典データセット | uspto-grants-1978_02 |
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| ORD ID | ord-0614c3ad5e564a9aa4f6399ba41cc9a6 |
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| 出典メモ | uspto-grants-1978_02 |
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