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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477047Generated: October 30, 2026

Ammonia → Methyl 5-(4-methoxyphenyl)pyridine-3-carboxylate

https://huagongshe.com/reaction/477047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 5-bromopyridine-3-carboxylateHCID 699336—
Reactant4-Methoxyphenyl boric acidHCID 14769994—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(4-methoxyphenyl)pyridine-3-carboxylateHCID 1476999524.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

2.16 g of methyl 5-bromonicotinate and 350 mg of tetrakis(triphenylphosphine)palladium were dissolved in 20 ml of toluene, and under a nitrogen current, 10 ml of a 2M aqueous solution of sodium carbonate and a suspension of 1.82 g of (4-methoxyphenyl)boric acid in 5 ml of methanol were added. The mixture was stirred at a bath temperature of 80° C. for 12 hours. To the reaction solution were added 100 ml of methylene chloride, 50 ml of a 2M aqueous solution of sodium carbonate and 5 ml of conc. aqueous ammonia to perform extraction. The organic layer was separated, and the solvent was evaporated. The residue was subjected to silica gel column chromatography. The column was eluted with a 3:7 mixture of ethyl acetate and hexane. The solvent was evaporated from the eluate to give 600 mg (yield 24.7%) of methyl 5-(4-methoxyphenyl)nicotinate as colorless needles having a melting point of 99° to 101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886822
Source datasetuspto-grants-1989_12
ORD IDord-0bc534388d90435daed9eaaade7b5428
Source noteuspto-grants-1989_12