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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750049Generated: October 29, 2026

Tetrahydrofuran → 1-Bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzene

https://huagongshe.com/reaction/1750049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium ethanethiolateHCID 4459711—
Reactant4-Bromo-3-fluorophenyl trifluoromethyl sulphideHCID 118035676—
SolventDimethylformamideHCID 6228—
Product1-Bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzeneHCID 11803556358.3%

Reaction Steps

0.21 g of sodium ethanethiolate (80%) was added to a mixture of 0.55 g of l-bromo-2-fluoro-4-trifluoromethylsulfanylbenzene and 4 ml of THF under ice cooling, and the mixture was stirred at room temperature for 30 minutes. 2 mL of DMF was added to the reaction mixture, and the mixture was stirred at 80° C. for 2 hours. A saturated aqueous sodium bicarbonate solution was added to the cooled reaction mixture, and the mixture was extracted with ethyl acetate and then dried with anhydrous sodium sulfate. The mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.37 g of 1-bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156838B2
Source datasetuspto-grants-2015_10
ORD IDord-09172ec6784f44fda24172d803031bb5
Source noteuspto-grants-2015_10