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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873073Generated: October 31, 2026

Butyl chloroformate → 5-n-Butoxycarbonylfuro[2,3-c]pyridine

https://huagongshe.com/reaction/1873073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl chloroformateHCID 61140—
Reactant3-Methylfuran-2-carbaldehyde-n-phenylimineHCID 9815443—
Reactantn-Butyl cyanoformateHCID 13809822—
SolventO-XyleneHCID 7237—
Product5-n-Butoxycarbonylfuro[2,3-c]pyridineHCID 1832419045.8%

Reaction Conditions

Temperature130 °C

Reaction Steps

n-Butyl cyanoformate(13.7 g, 0.108 mol) and 3-methylfuran-2-carbaldehyde-N-phenylimine(5.0 g, 27.0 mmol) were mixed at room temperature in xylene (25 mL) then heated to reflux at 120 to 140° C. with stirring. A xylene (15 mL) solution of 7.40 g (54.2 mol) of n-butyl chloroformate was added dropwise for an hour to the resulting mixture. After all the solution had been added, the reaction mixture was heated to reflux for 2 hours, it was allowed to cool to room temperature, and the solvent was distilled off to give 7.10 g of crude product. This product was purified by column chromatography on silica gel, giving 2.71 g (45.8% yield) of 5-n-butoxycarbonylfuro[2,3-c]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06111111
Source datasetuspto-grants-2000_08
ORD IDord-0d36bff69522468c8ebaccdf6f518f6b
Source noteuspto-grants-2000_08