関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Aluminum isopropoxide | HCID 11143 | — |
| 反応物 | 3,7beta-Dihydroxy-2-iodo-estra-1,3,5(10)-trien-17-one | HCID 11611293 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Cyclohexanone | HCID 7967 | — |
| 生成物 | 3-Hydroxy-2-iodo-estra-1,3,5(10)-triene-7,17-dione | HCID 11682983 | 63% |
反応手順
A solution of 206 mg (0.5 mmol) of 3,7β-dihydroxy-2-iodo-estra-1,3,5(10)-trien-17-one 14 in 15 ml of toluene and 4 ml of cyclohexanone was heated to 140° C. (oil bath temperature), and a solution of 400 mg of aluminum isopropylate in 10 ml of toluene was added drop by drop. In the meantime, a portion of the reaction mixture was distilled off. After complete addition of the aluminum isopropylate, it was refluxed for still another 5 hours. Then, the reaction solution was cooled and diluted with 80 ml of dichloromethane and 30 ml of potassium/sodium tartrate solution, and the resulting mixture was first stirred vigorously for 30 minutes before the organic phase was separated from the aqueous phase. The aqueous phase was finally extracted with dichloromethane (3×30 ml), and the combined organic phases were washed with a saturated NaCl solution, dried on sodium sulfate and concentrated by evaporation in a rotary evaporator. Flash chromatography (cyclohexane/ethyl acetate) yielded 129 mg (63%) of colorless crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07419972B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-ba0076bd14184a21bb44fc4c93e651f8 |
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| 出典メモ | uspto-grants-2008_09 |
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