Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425289Generated: October 30, 2026

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

https://huagongshe.com/reaction/425289

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 numberUS08106207B2
Source datasetuspto-grants-2012_01
ORD IDord-ec33a9391ca24958b9817d64a2509aa7
Source noteuspto-grants-2012_01