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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429693Generated: October 31, 2026

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

https://huagongshe.com/reaction/1429693

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 numberUS08940748B2
Source datasetuspto-grants-2015_01
ORD IDord-d0f3d40a8dcb4a2f93debd80346a0d5b
Source noteuspto-grants-2015_01