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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triclosan | HCID 5564 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Chloro-2-(2,4-dichlorophenoxy)phenyl prop-2-enoate | HCID 67346638 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06464961B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-541733ca58234a7d962701877abd65d5 |
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| Source note | uspto-grants-2002_10 |
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