関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thioglycolic Acid | HCID 1133 | — |
| 反応物 | 9alpha-Bromo-11beta-hydroxy-4-androstene-3,17-dione | HCID 11132685 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 11beta-Hydroxyandrost-4-ene-3,17-dione | HCID 94141 | 87% |
反応手順
A solution of 9α-bromo-11β-hydroxyandrost-4-ene-3,17-dione (III, 2.00 g), thioglycolic acid (2.0 ml) in THF (20 ml) and water (5 ml) is stirred under nitrogen at 20°-25°. A chromous sulfate solution (1.4 M, 5.5 ml) is added and the two-phase system is stirred. After four hours, another 4.5 ml of chromous sulfate solution is added and the mixture stirred overnight. The mixture is diluted with water and extracted with ethyl acetate. The ethyl acetate extracts are washed with water, a diluted sodium hydroxide solution, water and saline. The organic phase is dried over sodium sulfate and concentratd to a solid. The solid is crystallized from benzene-hexane to give a first crop of crystals of the title compound (1.38 g, 83.5% chemical yield) which are measured to be 99% pure as measured by GLC and is identical to an authentic sample.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04325881 |
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| 出典データセット | uspto-grants-1982_04 |
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| ORD ID | ord-6a9a5c473abc47e3bb54b8863a6f6350 |
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| 出典メモ | uspto-grants-1982_04 |
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