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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991379Generated: November 1, 2026

Triclosan → 5-Chloro-2-(2,4-dichlorophenoxy)phenyl prop-2-enoate

https://huagongshe.com/reaction/991379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriclosanHCID 5564—
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-(2,4-dichlorophenoxy)phenyl prop-2-enoateHCID 67346638—

Reaction Conditions

Temperature20 °C

Reaction Steps

Irgasan® DP300 5-chloro-2-(2,4-dichlorophenol)(triclosan), 23.5 g (0.081 mol) was dissolved in 300 ml of dry tetrahydrofuran in a 1-l jacketed kettle with agitator, addition funnel and reflux condenser. Then 10.6 ml of triethylamine was added to the solution with agitation. To the resulting solution was added dropwise 6.68 (0.0738 mol) g of acryloyl chloride. The reaction temperature was maintained at 20° C. with a circulating cooling bath. After the addition of acryloyl chloride was completed, the agitation and temperature conditions were maintained for 5 hours. Then the reaction product was kept overnight at room temperature, filtered to remove solid triethylamine hydrochloride and the filtrate rotovapped at room temperature under 100-110 mm Hg to concentrate the product. The remaining solution was dissolved in 100 ml heptane and washed with 5% Na2CO3 solution in Dl water until basic; then with Dl water until neutral. The heptane solution of the product was dried with MgSO4 in a refrigerator overnight, and filtered. The filtrate contained 25.3% triclosan acrylate as determined by bromination. FTIR spectrum confirmed the presence of the unsaturated ester of a phenol (1753 cm−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06464961B2
Source datasetuspto-grants-2002_10
ORD IDord-541733ca58234a7d962701877abd65d5
Source noteuspto-grants-2002_10