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HRID 128913作成日:2026年10月23日

Sodium Hydroxide → [4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acid

https://huagongshe.com/ja/reaction/128913

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2-Acetoxybenzoyl chlorideHCID 79668—
反応物Alendronate SodiumHCID 23681107—
触媒4-(Dimethylamino)pyridineHCID 14284—
触媒Tetrahexylammonium iodideHCID 75056—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物[4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acidHCID 86749102—

反応条件

温度0 °C

反応手順

3.18 g (9.8 mmoles ) of sodium trihydrogen 4-amino-1-hydroxybutylidenediphosphonate trihydrate are added in 30 ml of water to 1.8 g (45 mmoles) of sodium hydroxide, 100 mg of p-dimethylaminopyridine and 200 mg of tetrahexylammonium iodide. The resulting solution is cooled to 0° C., and added with 2.03 g (10.2 mmoles) of 2-acetoxybenzoic acid chloride dissolved in 10 ml of diethyl ether. The reaction mixture is stirred for 2 hours at room temperature, then it is extracted with ethyl ether and the aqueous solution is acidified with concentrated HCl under stirring, with cooling. [4-(2-Hydroxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acid precipitates, which is filtered, washed and dried at 70° C. and transformed into the title product by means of acetylation with acetic anhydride.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05466682
出典データセットuspto-grants-1995_11
ORD IDord-000990f6f7624768a2d521f93c51d0f7
出典メモuspto-grants-1995_11