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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889531Generated: November 1, 2026

Benzyl Bromide → Benzyl 5-cyano-2-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/889531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
ReactantDimethylacetamideHCID 31374—
Reactant5-Chloro-2-(trifluoromethyl)benzoic acidHCID 2773859—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystZincHCID 23994—
CatalystHCID 178454917HCID 178454917—
ProductBenzyl 5-cyano-2-(trifluoromethyl)benzoateHCID 6797034557%

Reaction Conditions

Temperature95 °C

Reaction Steps

Under a nitrogen atmosphere, to a solution of 5-chloro-2-(trifluoromethyl)benzoic acid (5.02 g, 22.35 mmol, 1.0 equiv) in DMA (45 mL), add zinc(II) cyanide (1.77 g, 15.07 mmol, 0.67 equiv), zinc dust (<10 μM, 330 mg, 5.05 mmol, 0.23 equiv), and bis(tri-tert-butylphosphino)palladium (540 mg, 1.06 mmol, 0.05 equiv). Stir the mixture under a nitrogen atmosphere at 95° C. for 9.5 hours. Add cesium carbonate (13.3 g, 40.82 mmol, 1.83 equiv), then benzyl bromide (3.0 mL, 25.15 mmol, 1.13 equiv), and stir under air at room temperature for 3.5 hours. Concentrate under reduced pressure, add water, and extract with EtOAc. Separate the organic phase and wash with saturated aqueous NaCl, dry over MgSO4, filter, and concentrate under reduced pressure. Subject the resulting crude material to flash chromatography on silica gel eluting with a 0-50% EtOAc/hexanes gradient to give the title compound (3.9 g, 57%). MS (m/z) 306 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252831B2
Source datasetuspto-grants-2012_08
ORD IDord-060b2d212a454d7caae7414001d59693
Source noteuspto-grants-2012_08