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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608039Generated: October 29, 2026

Ethyl Bromide → (1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl)ethyl sulfide

https://huagongshe.com/reaction/1608039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178505829HCID 178505829—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
Product(1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl)ethyl sulfideHCID 1455162081.4%

Reaction Steps

A solution of 1.75 g (0.0076 mole) of 1-(4-chloro-2-fluorophenyl)-1,4-dihydro-5H-tetrazol-5-thione, 0.57 ml (0.0076 mole) of bromoethane, and 1.6 g (0.012 mole) of potassium carbonate in 8 ml of acetone was stirred at room temperature for seven hours. The solvent was evaporated from the reaction mixture under reduced pressure leaving a residue. This residue was dissolved in diethyl ether and the organic solution was washed with water. The washed organic phase was dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to yield 1.6 g of (1-(4-chloro-2-fluorophenyl)-1H-tetrazol-5-yl) ethyl sulfide as a solid, m.p. 76°-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04868321
Source datasetuspto-grants-1989_09
ORD IDord-a280ca4d37d7426f87e652ddc7c69646
Source noteuspto-grants-1989_09