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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810682Generated: October 31, 2026

4-Bromothiophenol → HCID 67434549, compound

https://huagongshe.com/reaction/1810682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromothiophenolHCID 66049—
ReactantBromocyclopropaneHCID 78037—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
ProductHCID 67434549HCID 67434549—

Reaction Steps

To a degassed solution of potassium tert-butoxide (2.08 g, 18.51 mmol) in dry dimethylsulphoxide (6 mL), 4-bromo-benzenethiol (3.5 g, 18.5 mmol) was added and the mixture was stirred for 15 min at ambient temperature under nitrogen. Bromocyclopropane (4.4 mL, 55.5 mmol) was added afterwards and the reaction mixture was heated at 80° C. for 24 h in a sealed vessel. The mixture was cooled, diluted with ether (150 mL) and washed with water (100 mL). The aqueous layer was extracted with ether (3×50 mL). Combined organic extracts were finally dried with anhydrous magnesium sulfate. 1-Bromo-4-cyclopropyl-sulfanyl-benzene was obtained after evaporation of the solvent as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362016B2
Source datasetuspto-grants-2013_01
ORD IDord-65f3fb4031dd4fc9b74e108300b49a89
Source noteuspto-grants-2013_01