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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191691Generated: October 31, 2026

Pyridine → Methyl 6-Oxo-1-phenyl-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/1191691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 6-oxo-1,6-dihydropyridine-3-carboxylateHCID 416343—
CatalystCupric acetate monohydrateHCID 165397—
SolventDichloromethaneHCID 6344—
ProductMethyl 6-Oxo-1-phenyl-1,6-dihydropyridine-3-carboxylateHCID 1198907556%

Reaction Steps

Methyl-6-oxo-1,6-dihydropyridine-3-carboxylate (6.0 g, 39.22 mmol), phenylboronic acid (5.74 g, 47.06 mmol), copper(II) acetate monohydrate (11.76 g, 58.82 mmol), pyridine (6.32 mL, 78.43 mmol) and molecular sieves (4 Å, 6.0 g) in dichloromethane (100 mL) was stirred at ambient temperature for 12 hours and filtered. Standard extractive work up provided a crude residue which was purified by silica gel column chromatography (100-200 mesh) (1-2% methanol in chloroform) to give the title compound as a brown solid (5.0 g, 56%). m.p. 100-105° C.; 1H NMR (400 MHz, CDCl3) δ 3.86 (s, 3H), 6.63 (d, J=9.5 Hz, 1H), 7.36-7.55 (m, 5H), 7.91 (dd, J=2.5, 9.9 Hz, 1H), 8.23 (d, J=2.5 Hz, 1H); IR (KBr) υ 3058, 2924, 2854, 1721, 1675, 1540, 1446, 1313, 1271, 1103 cm−1; MS 230 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680123B1
Source datasetuspto-grants-2014_03
ORD IDord-6b865aa23ea043ea8f12c351972ed4f1
Source noteuspto-grants-2014_03