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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650909Generated: October 31, 2026

3-Methoxyphenol → 3-Chloro-2-p-methoxyphenoxy-5-trifluoromethylpyridine

https://huagongshe.com/reaction/1650909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyphenolHCID 9007—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3-Chloro-2-p-methoxyphenoxy-5-trifluoromethylpyridineHCID 19986019—

Reaction Conditions

Temperature60 °C

Reaction Steps

P-Methoxyphenol (1.5 g) was added to a suspension of sodium hydride (0.6 g 50% oil dispersion, washed with petroleum) in dry dimethyl sulphoxide (30 ml) and the mixture stirred for 15 minutes. A solution of the combined products (1.5 g) from several preparations carried out as described in paragraph (d), in dimethylsulphoxide (20 ml) was added to the reaction mixture and heated to 60° C. for four hours. A further amount of sodium hydride (0.3 g of 50% oil dispersion, washed with petroleum), and potassium carbonate (1.38 g) was added. Heating was continued for another 4 hours. The mixture was poured into ice and water, and extracted with ether (400 ml). The ether extracts were washed with water, dilute sodium hydroxide, and water, dried, and evaporated to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925947
Source datasetuspto-grants-1990_05
ORD IDord-691e331fb5bf4b1aa81f024fcbef8df3
Source noteuspto-grants-1990_05