関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Silica | HCID 24261 | — |
| 反応物 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 17alpha-Ethynyl-17beta-hydroxy-6,16-dimethyleneandrosta-4-en-3-one | HCID 13314929 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 17alpha-Acetyl-17beta-hydroxy-6,16-dimethyleneandrost-4-en-3-one | HCID 13314931 | — |
反応手順
9.0 Kg of 17α-ethynyl-17β-hydroxy-6,16-dimethyleneandrost-4-en-3-one is added to a reactor vessel, flushed with nitrogen until the oxygen content is less than 4%. 108 Liters (85.3 Kg) of acetone is added and the solution heated to 45° C. A catalyst solution (prepared by the addition of 0.72 liters conc. sulfuric acid to 10.8 liters of deionized water, followed by the addition of 576 grams of mercuric oxide, red powder to the dilute acid) is added to the reaction mixture and stirred at 45° C. until the reaction is complete, as monitored by TLC. The reaction mixture is cooled to less than 25° C. and 2.3 Kg Celite 545, 2.2 Kg sodium acetate and 20 liters of water added and mixture stirred for 15 min. The resulting crude product is filtered using a pot filter coated with Celite 545. The reactor is rinsed with 50 liters of acetone and filtered. The combined filtrate is concentrated under vacuum to about 50 liters, cooled to below 20° C. and stirred for 15 min. The slurry is filtered and the filter cake washed with 10 liters of acetone and 20 liters of water. The filter cake is dried in a vacuum oven at 50° C. to yield 17α-acetyl-17β-hydroxy-6,16-dimethyleneandrost-4-en-3-one (mercury content 10,500 ppm).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04588529 |
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| 出典データセット | uspto-grants-1986_05 |
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| ORD ID | ord-788cffc4036c42ba988d443c58839c4b |
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| 出典メモ | uspto-grants-1986_05 |
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