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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2,3-Epoxypropyl)phthalimideHCID 21601—
Reactant3-Amino-propanephosphonousHCID 9989268—
Catalystzinc(II)iodideHCID 9883512—
SolventHydrochloric AcidHCID 313—
SolventHexamethyldisilazaneHCID 13838—
Product3-Aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013863
Source datasetuspto-grants-1991_05
ORD IDord-28666e61568b4578a958ed3ee674779c
Source noteuspto-grants-1991_05