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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128935Generated: October 26, 2026

Methyl 2-Benzoylnicotinate → 2-Benzylnicotinic acid

https://huagongshe.com/reaction/128935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-BenzoylnicotinateHCID 19700681—
CatalystZincHCID 23994—
CatalystCopper SulfateHCID 24462—
SolventAmmonium HydroxideHCID 14923—
Product2-Benzylnicotinic acidHCID 1242873333%

Reaction Steps

Methyl 2-Benzoylnicotinate (2.41 g., 10 mmoles) was dissolved in 250 ml ammonium hydroxide. To this solution was carefully added a catalytic amount of copper (II) sulfate (approx. 100 mg) and zinc powder (7.0 g., 100 mmoles). The mixture was refluxed for 6 days and allowed to cool. The mixture was filtered (pad of celite), acidified to pH 5 with 1N HCl, exhaustively extracted with ethyl acetate, washed with brine, dried over sodium sulfate, filtered, concentrated under vacuum, and purified by column chromatography to give 0.70 grams (33% yield) of 2-benzylnicotinic acid as a white solid. Characteristic analytical data are as follows: mp 180°-182.5° C.; TLC in 20:1.8:0.2 (EtOAc/MeOH/HOAc); 1H NMR (DMSO-d6, 300 MHz) δ4.50 (s, 2H), 7.12-7.48 (m, 5H), 8.18 (dd, 1H, J=8.0, 1.6 Hz), 8.63 (dd, 1H, J=4.8, 1.5 Hz); 13C NMR (75 MHz, DMSO-d6) δ167.84, 160.17, 151.55, 139.85, 138.38, 128.75, 128.04, 126.37, 125.79, 121.57, 41.35, 39.76; mass spectrum (EI) , m/e 213.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466697
Source datasetuspto-grants-1995_11
ORD IDord-6b50fbd1237640d7822c62280e45391c
Source noteuspto-grants-1995_11