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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054328Generated: October 31, 2026

Water → 3-(Trifluoromethyl)pyridine-2-carbonitrile

https://huagongshe.com/reaction/2054328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-3-(trifluoromethyl)pyridineHCID 589833—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
Product3-(Trifluoromethyl)pyridine-2-carbonitrileHCID 22321574—

Reaction Steps

Dissolve 2-chloro-3-trifluoromethylpyridine (36.2 g, 0.2 moles) in DMF (350 mL) at room temperature. Add water (3.5 mL) and zinc cyanide (14 g, 0.12 moles) to the reaction mixture and degas with nitrogen for 15 minutes. Add catalyst Pd2(dba)3 (5.5 g, 3 mol %) and ligand DPPF (6.5 g, 6 mol %) to the mixture and then heat at 120° C. with stirring for 1 hour. Cool the reaction mixture in an ice bath and then add saturated ammonium chloride (200 mL), 28% ammonium hydroxide (50 mL) and water (50 mL). Stir the resulting reaction mixture in the ice bath for 1 hour and then dilute it EtOAc (300 mL). Separate the organic layer, extract the aqueous layer with EtOAc (3×300 mL), wash the combined organic layers with brine (2×200 mL) and dry (MgSO4). Filter the dried extract and concentrate under vacuum to afford crude product as dark brown oil. Purify the crude product by vacuum distillation to afford pure product as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329664B2
Source datasetuspto-grants-2008_02
ORD IDord-ef8d7a64e6e24f98b855605f2cf2c94e
Source noteuspto-grants-2008_02