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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128913생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-Acetoxybenzoyl chlorideHCID 79668—
반응물Alendronate SodiumHCID 23681107—
촉매4-(Dimethylamino)pyridineHCID 14284—
촉매Tetrahexylammonium iodideHCID 75056—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물[4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acidHCID 86749102—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05466682
출처 데이터셋uspto-grants-1995_11
ORD IDord-000990f6f7624768a2d521f93c51d0f7
출처 메모uspto-grants-1995_11