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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594311Generated: October 26, 2026

2,2,2-Trifluoroacetaldehyde hydrate → 4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/1594311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroacetaldehyde hydrateHCID 2781366—
Reactant4,4,4-Trifluoro-2-(triphenyl-lambda5-phosphanylidene)-butyric acid ethyl esterHCID 44541424—
SolventTetrahydrofuranHCID 8028—
Product4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)but-2-enoic acid ethyl esterHCID 7441005686%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 4,4,4-trifluoro-2-(triphenyl-λ5-phosphanylidene)-butyric acid ethyl ester (2.0 g, 4.65 mmol) in THF (5 mL) was added 1 mL of trifluoroacetaldehyde hydrate (tech.). The mixture was sealed in a pressure tube and heated at 100° C. for 3.5 h. After cooling to 23° C., the reaction mixture was eluted through a pad of silica gel (100 g) and Na2SO4 with Et2O (100 mL) to remove the by-products triphenylphosphine oxide and water. The eluent was distilled to remove Et2O and to afford the product as a colorless liquid (1.0 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300951B2
Source datasetuspto-grants-2007_11
ORD IDord-242a786be36b4cf79979a24eae5e641d
Source noteuspto-grants-2007_11