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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155472Generated: November 1, 2026

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

https://huagongshe.com/reaction/1155472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
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 numberUS04302242
Source datasetuspto-grants-1981_11
ORD IDord-418e7f24747544a38e9a7242269e13c0
Source noteuspto-grants-1981_11