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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393157Generated: October 30, 2026

Formamidine acetate → HCID 22648741, compound

https://huagongshe.com/reaction/393157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 86759544HCID 86759544—
SolventMethanolHCID 887—
ProductHCID 22648741HCID 2264874167%

Reaction Steps

46 g (0.85 mol) of sodium methoxide was dissolved in 700 ml of methanol, and 76 g (0.73 mol) of formamidine acetate was added, followed by stirring at room temperature for 15 minutes. Then, 146 g (0.61 mol) of 3-ethoxymethylene-1,1,1-trifluoro-5-methyl-2,4-hexanedione was added under cooling with ice, followed by heating and refluxing for further 2 hours. The solvent was distilled off under reduced pressure, and 1,000 ml of ice water was added, followed by extraction with ethyl acetate. The obtained organic layer was washed with water and then dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off under reduced pressure, and the obtained crude product was purified by silica gel column chromatography (developing solvent/n-hexane:ethyl acetate=6:1) to obtain 89 g (yield: 67%) of 5-isopropylcarbonyl-4-trifluoromethylpyrimidine as slightly yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806230B1
Source datasetuspto-grants-2004_10
ORD IDord-ce008569be8b4545848b2546ef24fe5a
Source noteuspto-grants-2004_10