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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2279933Erstellt: 26. Oktober 2026

Citric Acid → Methyl 6-formylpyridine-2-carboxylate

https://huagongshe.com/reaction/2279933

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
EduktDimethyl pyridine-2,6-carboxylateHCID 79549—
EduktSodium borohydrideHCID 4311764—
KatalysatorManganese dioxideHCID 14801—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
LösungsmittelChloroformHCID 6212—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 6-formylpyridine-2-carboxylateHCID 1257585029,4%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09133185B2
Quelldatensatzuspto-grants-2015_09
ORD IDord-e3509c0fb924418e93c3a95f6e4f05bc
Quellennotizuspto-grants-2015_09