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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279933Generated: October 26, 2026

Citric Acid → Methyl 6-formylpyridine-2-carboxylate

https://huagongshe.com/reaction/2279933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantDimethyl pyridine-2,6-carboxylateHCID 79549—
ReactantSodium borohydrideHCID 4311764—
CatalystManganese dioxideHCID 14801—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 6-formylpyridine-2-carboxylateHCID 1257585029.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

A suspension of dimethylpyridine-2,6-dicarboxylate (1.0 g, 5.12 mmol) in methanol (8 mL) and THF (3 mL) was heated at 75° C. until the solid was dissolved. NaBH4 (184 mg, 4.87 mmol) was then added portion-wise. The mixture was stirred at 70° C. for 1 h. The mixture was cooled to room temperature and 10% citric acid (1.6 mL) was added. The solution was filtered and the filtrate was evaporated to dryness, taken up in dichloromethane, dried over MgSO4 and the solvent was removed in vacuo. The residue was purified by silica gel chromatography, eluting with 0-100% EtOAc in isohexane, to provide a colourless oil which was then dissolved in toluene (20 mL) and chloroform (20 mL). MnO2 (194 mg, 22.2 mmol) was added and the mixture was stirred at room temperature for 18 h. The mixture was filtered through a pad of fluorosil, eluting with chloroform (30 mL) and the solvent was removed in vacuo to provide the title compound (249 mg, 29%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133185B2
Source datasetuspto-grants-2015_09
ORD IDord-e3509c0fb924418e93c3a95f6e4f05bc
Source noteuspto-grants-2015_09