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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274216Generated: October 25, 2026

Tetrahydrofuran → 3-Pyridinecarboxylic acid, 2-(4-methoxybenzoyl)-

https://huagongshe.com/reaction/274216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantFuro[3,4-b]pyridine-5,7-dioneHCID 69688—
ReactantHCID 178491912HCID 178491912—
SolventHydrochloric AcidHCID 313—
Product3-Pyridinecarboxylic acid, 2-(4-methoxybenzoyl)-HCID 1133436827.8%

Reaction Steps

To a THF (15 ml) solution of pyridine-2,3-dicarboxylic acid anhydride (1.0 g, 6.7 mmol) was added dropwise a THF solution of 4-methoxyphenylmagnesium bromide (0.89M, 8.0 ml, 7.1 mmol) at -78° C. The reaction mixture was stirred at the same temperature for 1 h and then a saturated aqueous solution of NH4Cl (20 ml) was added to quench the reaction. The reaction mixture was diluted with 1N HCl and extracted with AcOEt. The organic layer was dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (E. Merck, Kieselgel 60/chloroform:methanol=10:1) to give 2-(4-methoxyphenylcarbonyl)-3-pyridine carboxylic acid (479 mg) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389620
Source datasetuspto-grants-1995_02
ORD IDord-b52f5b32182147ada5b88506affe7b8f
Source noteuspto-grants-1995_02