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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873074Generated: November 2, 2026

Ammonium Chloride → 5-Acetylfuro(2,3-c)pyridine

https://huagongshe.com/reaction/1873074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl furo[2,3-c]pyridine-5-carboxylateHCID 11074225—
ReactantHCID 178467906HCID 178467906—
SolventTetrahydrofuranHCID 8028—
Product5-Acetylfuro(2,3-c)pyridineHCID 979390277%

Reaction Conditions

Temperature-30 °C

Reaction Steps

5-Ethoxycarbonylfuro[2,3-c]pyridine obtained in Example 2(3.82 g, 20.0 mmol) was dissolved in tetrahydrofuran (50 mL) and cooled to -30° C. To the cooled solution, 22.0 mL (22.0 mol) of 1.0 M solution of methyllithium/diethyl ether was added, and the solution was stirred for 2 hours at the same temperature, the reaction mixture was then poured into 100 mL of 5% ammonium chloride aqueous solution which had been cooled on ice, and the product was extracted twice with 100 mL of ethyl acetate. After washing with 100 mL of saturated sodium bicarbonate aqueous solution and 100 mL of saturated saline water, the extract was concentrated to give 3.12 g of crude product. This product was purified by column chromatography on silica gel, giving 2.48 g (77.0% yield) of 5-acetylfuro[2,3-c]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06111111
Source datasetuspto-grants-2000_08
ORD IDord-5dd61b5a322145c4a3de466276f956e9
Source noteuspto-grants-2000_08