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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041172Generated: November 3, 2026

Ethyl Bromide → Ethyl 4-cyanophenyl sulfide

https://huagongshe.com/reaction/2041172

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 numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-cc74c0172f564d5a97ae26690dc8f0fd
Source noteuspto-grants-2013_11