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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128913Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukt2-Acetoxybenzoyl chlorideHCID 79668—
EduktAlendronate SodiumHCID 23681107—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
KatalysatorTetrahexylammonium iodideHCID 75056—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt[4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acidHCID 86749102—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05466682
Quelldatensatzuspto-grants-1995_11
ORD IDord-000990f6f7624768a2d521f93c51d0f7
Quellennotizuspto-grants-1995_11