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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 801Generated: October 23, 2026

Ethanol → 4-Ethoxy-2-methylthio-6-[3-(trifluoromethyl)phenoxy]pyrimidine

https://huagongshe.com/en/reaction/801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-(Trifluoromethyl)phenolHCID 7376—
ReactantSodium hydrideHCID 24758—
Reactant4,6-Dichloro-2-(methylthio)pyrimidineHCID 80531—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-Ethoxy-2-methylthio-6-[3-(trifluoromethyl)phenoxy]pyrimidineHCID 19693868—

Reaction Steps

Ethanol (1.18 g, 0.0256×1.0 mol) and NaH (1.02 g, (ca.60% in mineral oil), 0.0256×1.0 mol) were dissolved in THF and 4,6-dichloro-2-methylthiopyrimidine (Compound No. VII-23)(5.0 g, 0.0256 mol) was added thereto. The resulting solution was stirred for about 30 minutes at room temperature. To this reaction solution, m-trifluoromethyl-phenol (6.23 g, 0.0256×1.5 mol), NaH (1.54 g, (ca.60% in mineral oil), 0.0256×1.5 mol), and KI (2.12 g, 0.0256×0.5 mol) dissolved in DMF were added. The resulting solution was refluxed for about 7 hours. The reaction solution was partitioned between ethyl acetate and aqueous saturated sodium hydrogen carbonate to separate an organic phase. The organic phase was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and concentrated, and thereafter purified on a silica gel column.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723412
Source datasetuspto-grants-1998_03
ORD IDord-0c41a886f892437a80e1ebfc69bc8999
Source noteuspto-grants-1998_03