関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzoic Acid | HCID 243 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | Isopregnanolone | HCID 92787 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3alpha-Benzoyloxy-5alpha-pregnan-20-one | HCID 54310207 | 92.8% |
反応手順
A mixture of 3β-hydroxy-5α-pregnan-20-one (285 mg, 318.5 g/m, 0.89 mmol), triphenylphosphine (258 mg, 262.3 g/m, 0.94 mmol), and benzoic acid (120 mg, 122.2 g/m, 0.98 mmol) was dissolved in 25 mL of tetrahydrofuran (freshly distilled). To this stirred reaction mixture at room temperature was added a solution of diisopropylazidodicarboxylate (DIAD) (0.194 mL, 1.027 g/ml, 202.2 g/m, 0.98 mmol) in 5 mL of tetrahydrofuran dropwise over a period of 5 minutes. The reaction was followed by thin layer chromatography (TLC) as the starting material was consumed. After two hours, the reaction mixture was concentrated under reduced pressure and filtered through a bed of silica gel (10 g) with a mixture of hexane/ethyl acetate (9:1). Fractions corresponding to the title compound were concentrated to give 349 mg of 3α-benzoyloxy-5α-pregnan-20-one (92% yield) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05591733 |
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| 出典データセット | uspto-grants-1997_01 |
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| ORD ID | ord-e08fb4dab4a244bcb5673f0b40e9b1f6 |
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| 出典メモ | uspto-grants-1997_01 |
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