Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Epoxybutane | HCID 7834 | — |
| Reactant | 3-Amino-propanephosphonous | HCID 9989268 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Hexamethyldisilazane | HCID 13838 | — |
| Product | HCID 9964348 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05013863 |
|---|
| Source dataset | uspto-grants-1991_05 |
|---|
| ORD ID | ord-f4459e131e0d49359f9334784fe668b2 |
|---|
| Source note | uspto-grants-1991_05 |
|---|