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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Acetoxybenzoyl chloride | HCID 79668 | — |
| Edukt | Alendronate Sodium | HCID 23681107 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Katalysator | Tetrahexylammonium iodide | HCID 75056 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | [4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acid | HCID 86749102 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05466682 |
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| Quelldatensatz | uspto-grants-1995_11 |
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| ORD ID | ord-000990f6f7624768a2d521f93c51d0f7 |
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| Quellennotiz | uspto-grants-1995_11 |
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