HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621056Generated: October 31, 2026
Allyl chloride → Butyl ethylpropenylphosphinate
https://huagongshe.com/reaction/1621056
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Butyl ethyiphosphonite | HCID 86614949 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Butyl ethylpropenylphosphinate | HCID 86657322 | 26% |
Reaction Steps
At room temperature, a three-neck flask equipped with stirrer and high-performance condenser is initially charged with 400 g of ethanol and this initial charge is devolatilized by stirring and passing nitrogen through it. Then, under nitrogen, 30 g (0.2 mol) of butyl ethylphosphonite (produced as in Example 3) are added, followed by the dropwise addition of initially 14.5 g (0.25 mol) of sodium ethoxide in ethanol and thereafter 19.1 g (0.25 mol) of allyl chloride. Following a reaction time of 5 hours, the reaction solution is passed for purification through a column charged with Deloxan® THP II and the solvent is removed in vacuo. The product (butyl ethylpropenylphosphinate) is purified by column chromatography to obtain 9.9 g (26% of theory) of butyl ethylpropenylphosphinate as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772519B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-d2c57119658e44c0af0fb632188fab5d |
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| Source note | uspto-grants-2014_07 |
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