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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372460Generated: November 1, 2026

Water → 1-Methyl-2-(propylsulfanyl)-4-[3-(trifluoromethyl)phenoxy]benzene

https://huagongshe.com/reaction/372460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Methyl-3-(propylsulfanyl)phenolHCID 14404504—
SolventDimethylacetamideHCID 31374—
Product1-Methyl-2-(propylsulfanyl)-4-[3-(trifluoromethyl)phenoxy]benzeneHCID 20327737—

Reaction Steps

4-Methyl-3-(n-propylthio)phenol (8.4 g, 0.05 mole) and 85.5 % potassium hydroxide (3.3 g, 0.05 mole) were dissolved in N,N-dimethylacetamide (50 ml) above 90° C. 3-Bromotrifluoromethylbenzene (11.2 g, 0.05 mole) and Cu powder (0.5 g, 0.008 mole) were added to this solution below 90° C and the mixture was stirred at 110°-160° C for 14 hr. After cooling, the reaction mixture was poured into water (150 ml) and extracted twice benzene. The combined organic layers were washed with 5 % sodium hydroxide solution, 5 % hydrochloric acid solution, and water, then dried over sodium fulfate. The solvent was removed, and the residue was purified by column chromatography on silica gel using n-hexane benzene (2 : 1). The yield of 4-methyl-3-n-propylthiophenyl 3-trifluoromethylphenyl ether was 8.9 g (54.8 %), colorless oil, nD25 1.5319. Anal. Found: C, 62.61; H, 5.33. Calcd. for C17H17F3OS : C, 62.56; H, 5.25 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091109
Source datasetuspto-grants-1978_05
ORD IDord-2fb17c4858b6423396c573dcf64c8754
Source noteuspto-grants-1978_05