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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068770Generated: November 4, 2026

Toluene → 5-(3,5-Difluorobenzyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/2068770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3,5-Difluorobenzyl bromideHCID 518896—
Reactant3-Cyano-4-fluorophenylboronic acidHCID 2757964—
CatalystHCID 178418397HCID 178418397—
SolventDiethyl EtherHCID 3283—
Product5-(3,5-Difluorobenzyl)-2-fluorobenzonitrileHCID 44134259129.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

3-Cyano-4-fluorophenylboronic acid (1.649 g, 10 mmol), powdered potassium phosphate (4.254 g, 20 mmol) and Pd(PPh3)4 (231 mg, 0.2 mmol) were charged in an oven-dried flask under argon atmosphere. The flask was evacuated and back-filled with argon thrice and then toluene (30 mL) and 3,5-difluorobenzyl bromide (1.295 mL, 10 mmol) were added by means of a syringe through a lattice stopper, under good stirring. The reaction mixture was heated to 100° C. in half an hour and maintained at that temperature for 1.5 hours. The black mixture was taken up with diethylether (200 mL), washed with saturated aqueous ammonium chloride (2×20 mL), brine (3×30 mL), dried over sodium sulphate and evaporated to dryness to afford 3.21 g of yellow oil. The crude was purified by flash chromatography on silica gel eluting with n-hexane/ethyl acetate 95:5 to yield 1.89 g (yield 76.4%) of whitish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299057B2
Source datasetuspto-grants-2012_10
ORD IDord-cd506a722532477885b3f6e4c424682c
Source noteuspto-grants-2012_10