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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050716Generated: November 3, 2026

1,2-Epoxybutane → HCID 9964348, compound

https://huagongshe.com/reaction/2050716

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 2.0 M 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-exchance chormatography on DOWEX® 50 W x 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 numberUS05013863
Source datasetuspto-grants-1991_05
ORD IDord-f4459e131e0d49359f9334784fe668b2
Source noteuspto-grants-1991_05