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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438903Generated: October 25, 2026

Vinyl Chloride → 1,1,3,3-Tetrachloropropane-1-phosphonic dichloride

https://huagongshe.com/reaction/1438903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl ChlorideHCID 6338—
Reactant(Trichloromethyl)phosphonic dichlorideHCID 277422—
ReactantTriethylazanium chlorideHCID 12698378—
CatalystBenzoinHCID 8400—
SolventAcetonitrileHCID 6342—
Product1,1,3,3-Tetrachloropropane-1-phosphonic dichlorideHCID 21399686926.1%

Reaction Steps

6.25 g (0.1 mole) vinyl chloride, 23.6 g (0.1 mole) trichloromethane phosphonic dichloride, 540 mg (2 mmole) ferric chloride hexahydrate, 412 mg (3 mmole) triethylammonium chloride, and 424 mg (2 mmole) benzoin were heated in 30 ml acetonitrile in an ampoule at 100° during 15 hours. After opening of the ampoule, and evaporating unconverted vinyl chloride, the reaction product was diluted with methylene chloride, washed twice with ice-cold 1N aqueous hydrochloric acid and dried on calcium chloride. The solvent was distilled at atmospheric pressure, and unconverted phosphonic dichloride sublimed at 25 mm and 120°. The remainder was fractionated in vacuo, giving 8.3 g 1,1,3,3-tetrachloropropane-1-phosphonic dichloride, bp/0.1: 66°-67°; containing 70.3% Cl (Calc. for C3H3Cl6OP: 71.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04057579
Source datasetuspto-grants-1977_11
ORD IDord-c0c8d4aa3a0b416aadc30656de867739
Source noteuspto-grants-1977_11