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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660032Generated: October 26, 2026

Trifluoroacetic acid → 4-Cyano-2-isobutylpyridine

https://huagongshe.com/reaction/660032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-CyanopyridineHCID 7506—
ReactantIsovaleric AcidHCID 10430—
ReactantSodium HydroxideHCID 14798—
CatalystSilver NitrateHCID 24470—
SolventChlorobenzene waterHCID 19815812—
Product4-Cyano-2-isobutylpyridineHCID 1464178654%

Reaction Conditions

Temperature0 °C

Reaction Steps

p-cyanopyridine (8.00 g, 76.8 mmol) was added to a 1:1 mixture of chlorobenzene/water (1.5 L) in a 2 L round-bottom flask. Isovaleric acid (21.74 g, 212.8 mmol), (NH4)2S2O8 (34.40 g, 150.7 mmol), trifluoroacetic acid (8.78 g, 77.0 mmol) and AgNO3 (1.040 g, 6.1 mmol) were added and the heterogeneous mixture was vigorously stirred and refluxed for 2 h. The reaction was cooled down to 0° C. and 8 M NaOH was added slowly until pH 9-10. The mixture was filtered through Celite and extracted with EtOAc (×3). The combined organic extracts were dried with MgSO4 and the solvent removed in vacuo. The dark-brown oil was purified via flash chromatography (1:4 EtOAc/Hexane) to give a brown oil (6.538 g, 54%);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084471B2
Source datasetuspto-grants-2011_12
ORD IDord-1bc1b13d81f64304970f530af7fa27c3
Source noteuspto-grants-2011_12