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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870808Generated: November 2, 2026

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

https://huagongshe.com/reaction/870808

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 numberUS08969576B2
Source datasetuspto-grants-2015_03
ORD IDord-a74299ea8b064510b73dc9d88a5525bb
Source noteuspto-grants-2015_03