HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050703Generated: October 27, 2026
Propylene Oxide → 3-Aminopropyl(propargyl)-phosphinic acid
https://huagongshe.com/reaction/2050703
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Amino-propanephosphonous | HCID 9989268 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 3-Aminopropyl(propargyl)-phosphinic acid | HCID 9855558 | — |
Reaction Steps
A suspension of 1,23 g (10 mmol) of 3-aminopropylphosphonous acid in 10.4 ml (50 mmol) of hexamethyldisilazane is heated to reflux under argon for 24 hours. 5 ml of diethylene glycol dimethyl ether are added to the clear solution obtained and the mixture is heated for addtitional 2 hours and then cooled to 0°. 8.5 ml (50 mmol) of N-ethyl-N,N-diisopropyl-amine are added, followed by slow addition of 3.8 ml (50 mmol) of propargyl bromide over a period of 40 minutes. The mixture is stirred for 1 hour at 0° and 4 hours at room temperature, filtered and evaporated under high vacuum. The residue is dissolved in 10 ml of dichloromethane and extracted with 3×10 ml of lN hydrochloric acid solution. The water layer is evaporated under high vacuum and the residue obtained dissolved in 4 ml of methanol at 0°. 20 ml of propylene oxide are added during a period of 1 hour, after which time a crude product precipitates. Chromatography (silicagel Merck 230-400 ASTM, methanol) followed by recrystallization (methanol/ether) yields 3-aminopropyl(propargyl)-phosphinic acid, m.p. 172-173°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05013863 |
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| Source dataset | uspto-grants-1991_05 |
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| ORD ID | ord-707b3a8dc99e4fa0a3d09146f541ee19 |
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| Source note | uspto-grants-1991_05 |
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