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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641470Generated: November 2, 2026

Acetic Anhydride → Ethyl 2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoate

https://huagongshe.com/reaction/1641470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 86640096HCID 86640096—
ProductEthyl 2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoateHCID 468575390%

Reaction Conditions

Temperature120 °C

Reaction Steps

In a 500 ml four-necked flask with stirrer, 78.3 g (0.425 mol) of trifluoroacetoacetate ethyl-(4,4,4-trifluoro)-3-oxobutyrate, 103.3 g (0.638 mol) of triethyl orthoformate and 130.0 g (1.275 mol) of acetic anhydride were mixed and heated at 120° C. for 6 hours. Then, at atmospheric pressure, initially the low-boiling components were removed and the product was then distilled under reduced pressure over a column. This gave 91.8 g (yield 90%) of the title compound as a colorless liquid of a purity>98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115012B2
Source datasetuspto-grants-2012_02
ORD IDord-4f08dc3c09544619abb77bf2aca29ec0
Source noteuspto-grants-2012_02