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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426227Generated: October 30, 2026

Triethylamine → Benzoic acid 2,3,6-trifluoro-pyridin-4-ylmethyl ester

https://huagongshe.com/reaction/426227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoic acid 3-chloro-2,5,6-trifluoro-pyridin-4-ylmethyl esterHCID 59184703—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductBenzoic acid 2,3,6-trifluoro-pyridin-4-ylmethyl esterHCID 5918476785.6%

Reaction Steps

Benzoic acid 3-chloro-2,5,6-trifluoro-pyridin-4-ylmethyl ester (4.52 g, 15 mmol), anhydrous ethanol (50 ml), 10% palladium on carbon (500 mg), and triethylamine (2.5 ml, 18 mmol) were placed into a 500 ml bottle. The mixture was hydrogenated under hydrogen atmosphere (50 psi) for 1.5 hr. The reaction mixture was filtered through celite pad and the pad was washed with ethanol. The combined filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography (eluent, ether:hexane (1:15)) to afford 3.43 g (85%) of benzoic acid 2,3,6-trifluoro-pyridin-4-ylmethyl ester as a white solid. m.p. 73-76° C.; 1H NMR (200 MHz, CDCl3) δ 5.52 (2H, s), 6.95 (1H, m), 7.30-7.70 (3H, m), 8.09-8.15 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106064B2
Source datasetuspto-grants-2012_01
ORD IDord-3c8e0d5ac3ed4e4d94001b05d4a9f075
Source noteuspto-grants-2012_01