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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486655Generated: November 1, 2026

(Trifluoromethyl)trimethylsilane → 2-Pyridinecarbonitrile, 5-(2,2,2-trifluoro-1-hydroxyethyl)-

https://huagongshe.com/reaction/1486655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
Reactant5-Formylpyridine-2-carbonitrileHCID 10986263—
SolventTetrahydrofuranHCID 8028—
Product2-Pyridinecarbonitrile, 5-(2,2,2-trifluoro-1-hydroxyethyl)-HCID 6708593039.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a −78° C. solution of 5-formylpicolinonitrile (1.0 g, 7.58 mmol) and tetrabutylammonium triphenyldifluorosilicate (4.9 g, 9.10 mmol) in 60 mL of THF was added a solution of trimethyl(trifluoromethyl)silane (1.62 g, 114 mmol). The mixture was stirred for 20 min at −78° C. Then the cooling bath was changed to an ice bath. After stirring for another 30 min, the reaction was quenched with sat. NH4Cl(aq.). The mixture was extracted with EtOAc (3×). The organic layer was washed with sat. NaHCO3(aq.), brine, then dried (MgSO4) and concentrated. The product 5-(2,2,2-trifluoro-1-hydroxyethyl)picolinonitrile (600 mg) was obtained by silica gel chromatography (elution with 0-40% EtOAc/Hex).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428475B2
Source datasetuspto-grants-2016_08
ORD IDord-fe8f234eba094926819ea2c440395bb5
Source noteuspto-grants-2016_08