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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128913Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Acetoxybenzoyl chlorideHCID 79668—
ReactantAlendronate SodiumHCID 23681107—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
CatalystTetrahexylammonium iodideHCID 75056—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product[4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acidHCID 86749102—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466682
Source datasetuspto-grants-1995_11
ORD IDord-000990f6f7624768a2d521f93c51d0f7
Source noteuspto-grants-1995_11