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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013940Generated: October 31, 2026

Thiophenol → 4-Bromo-2-(phenylsulfanyl)benzonitrile

https://huagongshe.com/reaction/1013940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
SolventDimethylformamideHCID 6228—
Product4-Bromo-2-(phenylsulfanyl)benzonitrileHCID 5772530296.8%

Reaction Steps

Sodium hydride (2.40 g, 60 mmol) (60% by wt) was weighed into a flask and washed with several hexane rinsings. The hexanes were decanted and discarded and 20 mL DMF was added to the flask. A DMF-solution of benzenethiol (5.1 mL, 50 mmol in 50 mL DMF) was added dropwise to the NaH mixture and stirred at room temperature. To 4-bromo-2-fluoro-benzonitrile (10.0 g, 50 mmol) in 40 mL DMF) was added benzenethiophenoxide (described above), dropwise, over 30 minutes. Upon complete addition, the reaction was stirred at room temperature for 20 min. At that time, the mixture was poured into cold 1 N NaOH. A precipitate formed and was collected by vacuum filtration to give 14.0 g (48.4 mmol) of Compound 1h.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982042B2
Source datasetuspto-grants-2011_07
ORD IDord-b417c2a775964e92be31a3ef95e1aeef
Source noteuspto-grants-2011_07