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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372459Generated: October 31, 2026

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

https://huagongshe.com/reaction/372459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant(Bromomethyl)(phenyl)sulfaneHCID 1501913—
Reactant4-Methyl-3-(propylsulfanyl)phenolHCID 14404504—
SolventDimethylacetamideHCID 31374—
Product1-Methyl-4-[4-(methylsulfanyl)phenoxy]-2-(propylsulfanyl)benzeneHCID 20327738—

Reaction Steps

4-Methyl-3-(n-propylthio)phenol (4.0 g, 0.02 mole) and 85.5 % potassium hydroxide (1.4 g, 0.02 mole) were dissolved in N,N-dimethylacetamide (40 ml) above 90° C. 4-Bromomethylthiobenzene (4.0 g, 0.02 mole) and Cu powder (0.5 g, 0.008 mole) were added to this solution below 90° C and the mixture was stirred at 120° - 160° C for 14 hr. After cooling, the reaction mixture was poured into water (100 ml) and extracted twice with benzene. The combined organic layers were washed with 5 % sodium hydroxide solution, 5 % hydrochloric acid solution, and water, then dried over sodium sulfate. The solvent was removed, and the residue was distilled under reduced pressure. The yield of 4-methyl-3-n-propylthiophenyl 4-methylthiophenyl ether was 4.1 g (61.5 %), colorless oil, bp 188° - 190° C/2 mmHg. Anal. Found: C, 67.12; H, 6.59. Calcd. for C17H20OS2 : C, 67.06; H, 6.62 %

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04091109
Source datasetuspto-grants-1978_05
ORD IDord-115dad9d874248fc975338b82261d68b
Source noteuspto-grants-1978_05