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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1463642Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1463642

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(2,3-Epoxypropyl)phthalimideHCID 21601—
Edukt3-Amino-propanephosphonousHCID 9989268—
Katalysatorzinc(II)iodideHCID 9883512—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelHexamethyldisilazaneHCID 13838—
Produkt3-Aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acidHCID 9901853—

Reaktionsschritte

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 2.0M 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-exchange chromatography on DOWEX® 50 W×8 (14-40 mesh) to give 3-aminopropyl(2-hydroxy-3-phthalimido-propyl)phosphinic acid, m.p. 268°-71°, as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05300679
Quelldatensatzuspto-grants-1994_04
ORD IDord-206d99e2118c4be8bb4a6c25b3cf2e6b
Quellennotizuspto-grants-1994_04