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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729152Generated: October 25, 2026

N-(2,3-Epoxypropyl)phthalimide → 3-Aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acid

https://huagongshe.com/reaction/729152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2,3-Epoxypropyl)phthalimideHCID 21601—
ReactantIodide IonHCID 30165—
Reactant3-Amino-propanephosphonousHCID 9989268—
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 anhydrouszinc 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 roomtemperature for 1 hour and the water removed in vacuo to give an oily solid. This is dissolved in 25 ml of 2.0M aqueous hydrochloric acid and washed with dichloromethane and ether. Removal of the water at 40° in vacuo affords a brown solid which is purified by ion-exchange chromatography on DOWEX® 50 W ×8 (14-40 mesl) to give 3-aminopropyl(2-hydroxy-3-phthalimido-propyl) phosphinic acid, m.p. 268°-71°, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051524
Source datasetuspto-grants-1991_09
ORD IDord-8743a177ebb84d9586cc46acffc17242
Source noteuspto-grants-1991_09