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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770109Generated: October 26, 2026

Acetic Anhydride → Ethyl 3-ethoxy-2-(2,4,5-trifluoro-3-methoxybenzoyl)acrylate

https://huagongshe.com/reaction/1770109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl 3-oxo-3-(2,4,5-trifluoro-3-methoxyphenyl)propanoateHCID 10588473—
ReactantEthylorthoformateHCID 53630039—
ProductEthyl 3-ethoxy-2-(2,4,5-trifluoro-3-methoxybenzoyl)acrylateHCID 5454884098.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of ethyl-3-methoxy-2,4,5-trifluorobenzoylacetate (500 mg, 1.8 mmol), ethyl orthoformate (0.45 mL, 2.72 mmol) and acetic anhydride (460 mg, 4.5 mmol, 2.5 eq) was stirred at 110° C. for 12 hours and the excess reagents were removed by distillation under high vacuum (0.1 mmHg) to give 590 mg of a yellow-orange oil. This material was used directly in the next step without further purification or characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05385913
Source datasetuspto-grants-1995_01
ORD IDord-3ee6a5d6d6b74eb58ddc853776f7a5b1
Source noteuspto-grants-1995_01