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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930464Generated: October 30, 2026

Trifluoroacetic acid → 5-Cyano-3-methylpyridine-2-carboxylic acid

https://huagongshe.com/reaction/930464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant5-Cyano-3-methyl-pyridine-2-carboxylic acid tert-butyl esterHCID 66665826—
SolventDichloromethaneHCID 6344—
Product5-Cyano-3-methylpyridine-2-carboxylic acidHCID 6666584694%

Reaction Steps

To a solution of tert-butyl 5-cyano-3-methylpicolinate (synthesized according to procedure described in WO2012095521; 4.18 g, 19.15 mmol) in dichloromethane (96 ml) was added TFA (Aldrich, 148 ml, 1915 mmol). The reaction mixture was stirred at room temperature for 2 hrs. The reaction mixture was concentrated under reduced pressure and the residue was triturated with EtOAc. The yellow slurry was concentrated under reduced pressure. The residue was triturated with 30 mL of methyl tert-butyl ether (30 mL) and of hexanes (50 mL) to yield 5-cyano-3-methylpicolinic acid (2.91 g, 17.95 mmol, 94% yield) as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-a27e4c270ad54d169bb607bf17bf96ec
Source noteuspto-grants-2016_03