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HRID 65344作成日:2026年10月25日

Acetone → Anecortave Acetate

https://huagongshe.com/reaction/65344

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Potassium HydroxideHCID 14797—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物17alpha-Hydroxy-20-phenoxypregna-4,9(11),20-trien-3-oneHCID 13823825—
反応物Potassium hydroxy sulfiteHCID 23707502—
溶媒WaterHCID 962—
溶媒Toluene methylene chlorideHCID 21877217—
生成物Anecortave AcetateHCID 111332—

反応条件

温度15 °C

反応手順

17α-hydroxy-20-phenoxypregna-4,9(11),20-trien-3-one (4.05 grams, 10 mmoles) is slurried with 210 ml of an aqueous pH 8 potassium phosphate buffer (0.5M in PO4 ≡), 20 ml of acetone, 40 ml of toluene/methylene chloride (3:2) and n-tetrabutylammonium bromide is (0.645 grams, 2.0 mmole) added. The pH is adjusted to 7.0 to 8.0 and the mixture cooled to 15° C. and an OXONE® solution is (18.4 gms, 30 mmoles dissolved in 65 ml of water) added dropwise by an addition funnel while stirring and maintaining pH at 7.0 to 8.0 by addition of a 30% potassium hydroxide solution. The reaction is worked up by separating the layers and replacing the organic solvent with toluene to a volume of 100 ml so as to remove water. After cooling to 10° C., 3 ml of glacial acetic acid is added. The product is isolated by replacing the toluene with acetone and filtering to obtain 3.12 g of 17α-hydroxy-21-acetoxypregna-4,9(11)-diene-3,20-dione.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04613463
出典データセットuspto-grants-1986_09
ORD IDord-a9ec3ad44eae4e0c8fd779ec69e81f7c
出典メモuspto-grants-1986_09