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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911283Generated: October 30, 2026

Ethyl Bromide → Ethyl 4-cyanophenyl sulfide

https://huagongshe.com/reaction/911283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPotassium CarbonateHCID 11430—
Reactant4-ThiobenzonitrileHCID 585058—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-cyanophenyl sulfideHCID 2126289183%

Reaction Steps

Combine 4-mercapto-benzonitrile (0.4 g, 2.96 mmol), bromoethane (1.4 mL, 8.88 mmol) and potassium carbonate (3.3 g, 23.7 mmol) in anhydrous DMF (7 mL) and heat at 60° C. for 17 h. Cool the reaction mixture to ambient temperature and partition between brine (20 mL) and EtOAc (20 mL). Separate the organic layer, dry over anhydrous Na2SO4 and concentrate. Purify by chromatography on silica gel eluting with hexane/EtOAc (1:0, 9:1 and 4:1) to obtain the desired intermediate as a colorless oil (0.4 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-c3aa0a5f7356458d8baf58e3291c277f
Source noteuspto-grants-2011_09