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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621057Generated: November 1, 2026

Allyl chloride → Butyl ethylpropenylphosphinate

https://huagongshe.com/reaction/1621057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantSodium ethoxideHCID 2723922—
ReactantButyl ethyiphosphoniteHCID 86614949—
CatalystHCID 178418751HCID 178418751—
SolventEthanolHCID 702—
ProductButyl ethylpropenylphosphinateHCID 8665732266%

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, 3.27 g (5 mmol) of bis(triphenylphosphine)nickel dichloride and 30 g (0.2 mol) of butyl ethylphosphonite (produced as in Example 2) 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 is purified by column chromatography to obtain 25.1 g (66% 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-1d54976d40bc482da6a22edf0b3ac499
Source noteuspto-grants-2014_07