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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277577Generated: October 31, 2026

Trimethylsilyl cyanide → 2-(3-Chloro-2-fluorophenyl)acetonitrile

https://huagongshe.com/reaction/2277577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant1-(Bromomethyl)-3-chloro-2-fluorobenzeneHCID 522827—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventAcetonitrileHCID 6342—
Product2-(3-Chloro-2-fluorophenyl)acetonitrileHCID 277372488%

Reaction Steps

To a solution of 1-chloro-3-bromomethyl-2-fluoro-benzene (2.22 g, 10 mmol) in CH3CN (30 mL) was added trimethylsilyl cyanide (1.5 mL) and TBAF (1M in THF, 12 mmol, 12 mL). The resulting reaction mixture was heated at reflux temperature for 30 min. After cooling to room temperature, the volatiles were evaporated under reduced pressure. The residue was partitioned between EtOAc and water. The organic layer was then washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash column chromatography to give the title compound (1.48 g, 88%). MS: 170.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133158B2
Source datasetuspto-grants-2015_09
ORD IDord-e99838d0abde499188cad416617c0b87
Source noteuspto-grants-2015_09