Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161510Generated: October 28, 2026

Tetrahydrofuran → HCID 58706315, compound

https://huagongshe.com/reaction/1161510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
ReactantN-FormylmorpholineHCID 20417—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
ProductHCID 58706315HCID 58706315—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of the 5.28 g of light yellow oil in 80 ml of THF there was added dropwise 9.07 ml of n-butyllithium (2.64 M, hexane solution) at −78° C. over a period of 20 minutes. After stirring at −78° C. for 3 hours, 4.59 ml of N-formylmorpholine was added. After further stirring at −78° C. for 20 minutes, the temperature was slowly allowed to rise to room temperature. Saturated aqueous ammonium chloride was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate) to give 5-ethoxy-6-methoxypyridine-3-carbaldehyde (2.23 g) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-4f4d44e77883416fb5a7c5aaac407bfb
Source noteuspto-grants-2010_10