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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202520Generated: November 2, 2026

Hydrochloric Acid → 3-Amino-5-(trifluoromethyl)pyridine-2-carboxylic acid

https://huagongshe.com/reaction/2202520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-amino-5-(trifluoromethyl)pyridine-2-carboxylateHCID 58964419—
SolventMethanolHCID 887—
Product3-Amino-5-(trifluoromethyl)pyridine-2-carboxylic acidHCID 46315205—

Reaction Steps

To a stirring solution of 3-Amino-5-trifluoromethyl-pyridine-2-carboxylic acid methyl ester (Intermediate A3) (1 g, 4.54 mmol) in MeOH (20 ml) was added 2M NaOH (0.182 g, 4.54 mmol). The orange solution was stirred at RT for 1 minute and then into water (10 ml). The solution was acidified to pH1 with the addition of 1M HCl and the product was extracted with EtOAc (150 ml). The organic portions were combined, washed with brine (50 ml), dried over MgSO4 and concentrated in vacuo to afford the title compound as an orange solid; LC-MS Rt=0.82 mins [M+H]+ 207.1 (Method 2minLC_v002); 1H NMR (400 MHz, DMSO-d6) δ 13.9 (1H, broad hump), 8.11 (1H, s), 7.59 (1H, s), 7.08 (2H, broad hump) (trace of EtOAc present but correlates to proposed structure).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365552B2
Source datasetuspto-grants-2016_06
ORD IDord-15b5d5babc5a4c0dbac5b1efb2066a7f
Source noteuspto-grants-2016_06