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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178497027 | HCID 178497027 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | methyl 8-bromo-2-(ethylthio)-4-oxo-4H-chromene-6-carboxylate | HCID 58235026 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09029374B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-7b27232190d74e81a6b1aa808916a62f |
|---|
| Source note | uspto-grants-2015_05 |
|---|