HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050722Generated: October 30, 2026
N-(2,3-Epoxypropyl)phthalimide → 3-Aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acid
https://huagongshe.com/reaction/2050722
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(2,3-Epoxypropyl)phthalimide | HCID 21601 | — |
| Reactant | 3-Amino-propanephosphonous | HCID 9989268 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Hexamethyldisilazane | HCID 13838 | — |
| Product | 3-Aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acid | HCID 9901853 | — |
Reaction Steps
A suspension of 2.46 g of 3-aminopropylphosphonous acid in 20 ml of hexamethyldisilazane is heated to reflux under an inert atmosphere for 24 hours after which a clear solution results. The excess hexamethyldisilazane is removed by distillation at atmospheric pressure under a slight positive pressure of inert gas to afford a colourless oil. The oil is cooled to circa 66° and treated with 0.64 g of anhydrous zinc iodide and 4.62 g of N-(2,3-epoxypropyl)phthalimide. An exothermic reaction occurs. The reaction mixture is refluxed for 6 hours after which time thin layer chromatography indicates the reaction to be complete. The reaction mixture is filtered and the filtrate evaporated to dryness in vacuo at 40°. The residue is dissolved in water and stirred at room temperature for 1 hour and the water removed in vacuo to give an oily solid. This is dissolved in 25 ml of 2.0 M aqueous hydrochloric acid and washed with dichlormethane and ether. Removal of the water at 40° in vacuo affords a brown solid which is purified by ion-exchance chromatography on DOWEX® 50 W x 8 (14-40 mesh) to give 3-aminopropyl(2-hydroxy3-phthalimido-propyl)phosphinic acid, m.p. 268°-71°, as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05013863 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-28666e61568b4578a958ed3ee674779c |
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| Source note | uspto-grants-1991_05 |
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