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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612697Generated: October 30, 2026

1,2-Epoxybutane → HCID 9964348, compound

https://huagongshe.com/reaction/1612697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-EpoxybutaneHCID 7834—
Reactant3-Amino-propanephosphonousHCID 9989268—
Catalystzinc(II)iodideHCID 9883512—
SolventHydrochloric AcidHCID 313—
SolventHexamethyldisilazaneHCID 13838—
ProductHCID 9964348HCID 9964348—

Reaction Steps

A suspension of 2.46 g of 3-aminopropylphosphonous acid in 20 ml of hexamethyldisilazane is heated to reflux under an inert gas 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 40° and treated with 0.64 g of anhydrous zinc iodide and 25 ml of 1,2-epoxybutane. An exothermic reaction occurs and the epoxybutane refluxes. Reflux is continued 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 some 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 mesh) to give 3-aminopropyl(-2-hydroxybutyl)phosphinic acid, m.p. 184°-185°. as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190933
Source datasetuspto-grants-1993_03
ORD IDord-aa8733a11e5a41349a9b3834546b4c20
Source noteuspto-grants-1993_03