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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394271Generated: October 29, 2026

Trifluoroacetamidine → Ethyl 2,4-bis(trifluoromethyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/2394271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetamidineHCID 2776882—
ReactantEthyl 2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoateHCID 4685753—
SolventEthanolHCID 702—
ProductEthyl 2,4-bis(trifluoromethyl)pyrimidine-5-carboxylateHCID 1049355839%

Reaction Steps

A solution of ethyl ethoxymethylene-4,4,4-trifluoroacetoacetate (15 g, 62.5 mmol) and trifluoroacetamidine (12.6 g, 112.5 mmol) in EtOH (50 mL) was heated at reflux for 24 h under N2. The reaction mixture was cooled and concentrated. Chromatography (SiO2, 20% EtOAc/hexane) afforded ethyl-2,4-bis (trifluoromethyl)pyrimidine-5-carboxylate as an oil (7.0 g, 39%), 1HNMR (CDCl3) δ 9.37 (s, 1H), 3.70 (q, 2H), 1.27 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811428
Source datasetuspto-grants-1998_09
ORD IDord-4baead46329c48d7a417b6270e76d3e4
Source noteuspto-grants-1998_09