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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325829Generated: October 29, 2026

Dimethyl Sulfoxide → Propyl 2-[5-(2-nitro-4-trifluoromethylphenoxy)-2-methylthiophenoxy]propionate

https://huagongshe.com/reaction/325829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
ReactantPropyl 2-bromopropanoateHCID 527505—
Reactant5-(2-Nitro-4-trifluoromethylphenoxy) 2-(methylthio)phenolHCID 20462817—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
ProductPropyl 2-[5-(2-nitro-4-trifluoromethylphenoxy)-2-methylthiophenoxy]propionateHCID 131713485—

Reaction Steps

5-(2-Nitro-4-trifluoromethylphenoxy)-2-(methylthio)phenol (0.05 mole), potassium carbonate (0.2 mole), propyl 2-bromopropionate (0.08 mole) and dimethylsulfoxide (200 ml) are charged into a 500 ml glass reaction flask equipped with a mechanical stirrer. The reaction mixture is stirred at room temperature for a period of about 8 hours. After this time the mixture is poured into 500 ml of water. The resulting mixture is extracted three times with 100 ml portions of methylene chloride. The extracts are then combined, washed with water and thereafter dried. The dried solution is then stripped of solvent under reduced pressure to leave a residue. The residue is subjected to chromatography using a clay column and hexane/ethyl acetate mixtures as the eluant. The fractions containing the product are combined and stripped of solvent to yield the desired product propyl 2-[5-(2-nitro-4-trifluoromethylphenoxy)-2-methylthiophenoxy]propionate as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443248
Source datasetuspto-grants-1984_04
ORD IDord-542b03ca93174f40838a0ec31060b92c
Source noteuspto-grants-1984_04