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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225003Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 1474127, compound

https://huagongshe.com/reaction/225003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Dichloro-5-(trifluoromethyl)pyridineHCID 112234—
SolventWaterHCID 962—
ProductHCID 1474127HCID 147412760.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a flask, 64 g of 2,3-dichloro-5-trifluoromethyl pyridine, 250 ml of dimethyl sulfoxide, 81.8 g of anhydrous potassium carbonate and 33.4 g of phenol were charged. The flask was heated in an oil bath at 100° C. to react them with stirring for 4 hours. The reaction mixture was poured into suitable amount of water and the reaction product was extracted with methylene chloride. The extracted phase was washed with water, with 5% sodium hydroxide aqueous solution and then, with water and dried over anhydrous sodium sulfate. Methylene chloride was distilled off under a reduced pressure and the residue was distilled to obtain 49 g of 2-phenoxy-3-chloro-5-trifluoromethyl pyridine. The product was mixed with 100 ml of 98% sulfuric acid and the mixture was cooled with ice water. A mixture of 11.3 g of 60% nitric acid and 30 ml of 98% sulfuric acid was added dropwise to the sulfuric acid solution of the reaction product at a temperature of 0° to 10° C. A mild exothermic reaction was performed. After the reaction, the reaction mixture was poured into suitable amount of ice water and neutralized with 10% sodium hydroxide aqueous solution. The reaction product was extracted with methylene chloride. The extracted phase was dried over anhydrous sodium sulfate. Methylene chloride was distilled off under a reduced pressure to obtain 38.5 g of the object compound having a melting point of 90° to 91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235621
Source datasetuspto-grants-1980_11
ORD IDord-9be5b99f44dd4ed7875adb8502d8b622
Source noteuspto-grants-1980_11