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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249146Generated: November 1, 2026

4-Chlorophenol → 1-(4-Chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-one

https://huagongshe.com/reaction/1249146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorophenolHCID 4684—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-3-methyl-3-trifluoromethylthio-butan-2-oneHCID 13117301—
SolventAcetoneHCID 180—
Product1-(4-Chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-oneHCID 1311730273%

Reaction Steps

26 g (0.21 mol) of 4-chlorophenol and 42 g (0.3 mol) of potassium carbonate were introduced into 250 ml of acetone. 53 g (0.2 mol) of 1-bromo-3-methyl-3-trifluoromethylthio-butan-2-one in 50 ml of acetone were slowly added dropwise to the mixture, under reflux. After the end of the addition, the mixture was stirred under reflux for 12 hours and was filtered, and the filtrate was concentrated. The residue was taken up in 500 ml of methylene chloride, the solution was extracted by shaking with water and sodium bicarbonate solution, and the organic phase was dried over sodium sulphate and concentrated. The residue was distilled in vacuo. 45.3 g (73% of theory) of 1-(4-chlorophenoxy)-3-methyl-3-trifluoromethylthio-butan-2-one of boiling point 105° C./0.4 mbar were obtained. ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04629732
Source datasetuspto-grants-1986_12
ORD IDord-ea417a378649483ba1547893643a1a22
Source noteuspto-grants-1986_12