Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621056Generated: October 31, 2026

Allyl chloride → Butyl ethylpropenylphosphinate

https://huagongshe.com/reaction/1621056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantSodium ethoxideHCID 2723922—
ReactantButyl ethyiphosphoniteHCID 86614949—
SolventEthanolHCID 702—
ProductButyl ethylpropenylphosphinateHCID 8665732226%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772519B2
Source datasetuspto-grants-2014_07
ORD IDord-d2c57119658e44c0af0fb632188fab5d
Source noteuspto-grants-2014_07