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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Acetoxybenzoyl chloride | HCID 79668 | — |
| Reactant | Alendronate Sodium | HCID 23681107 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Catalyst | Tetrahexylammonium iodide | HCID 75056 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | [4-(2-Acetoxybenzoyl)-amino-1-hydroxybutylidene]-diphosphonic acid | HCID 86749102 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05466682 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-000990f6f7624768a2d521f93c51d0f7 |
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| Source note | uspto-grants-1995_11 |
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