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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572801Generated: October 30, 2026

Iodoethane → methyl 8-bromo-2-(ethylthio)-4-oxo-4H-chromene-6-carboxylate

https://huagongshe.com/reaction/572801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178497027HCID 178497027—
SolventAcetoneHCID 180—
Productmethyl 8-bromo-2-(ethylthio)-4-oxo-4H-chromene-6-carboxylateHCID 5823502672%

Reaction Conditions

Temperature60 °C

Reaction Steps

Iodoethane (2.04 mL, 25.54 mmol), was added to a stirred suspension of methyl 8-bromo-4-hydroxy-2-thioxo-2H-chromene-6-carboxylate (2.3 g, 7.30 mmol) and potassium carbonate (1.21 g, 8.76 mmol) in acetone (100 mL) under argon. The resulting mixture was stirred at 60° C. for 2 hrs. The mixture was concentrated in vacuo, and the residue was partioned between water and DCM. The aqueous layer was extracted into DCM, and the organic extracts were combined, washed with brine, dried over magnesium sulfate and evaporated. The crude product was purified by flash chromatography on silica gel eluting with 0 to 10% ethyl acetate in DCM. The solvent was evaporated to dryness to afford methyl 8-bromo-2-(ethylthio)-4-oxo-4H-chromene-6-carboxylate (1.8 g, 72%) as an orange solid. Mass Spectrum: M+H+ 343.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029374B2
Source datasetuspto-grants-2015_05
ORD IDord-7b27232190d74e81a6b1aa808916a62f
Source noteuspto-grants-2015_05