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HRID 280078作成日:2026年10月26日

Silica → 17alpha-Acetyl-17beta-hydroxy-6,16-dimethyleneandrost-4-en-3-one

https://huagongshe.com/reaction/280078

反応式

関与物質

役割名称HCID仕込み量
反応物SilicaHCID 24261—
反応物Sodium AcetateHCID 517045—
反応物17alpha-Ethynyl-17beta-hydroxy-6,16-dimethyleneandrosta-4-en-3-oneHCID 13314929—
溶媒WaterHCID 962—
生成物17alpha-Acetyl-17beta-hydroxy-6,16-dimethyleneandrost-4-en-3-oneHCID 13314931—

反応条件

温度45 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04588529
出典データセットuspto-grants-1986_05
ORD IDord-788cffc4036c42ba988d443c58839c4b
出典メモuspto-grants-1986_05