HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-bromo-1-(2H-chromen-3-yl) ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(2H-1-Benzopyran-3-yl)ethanone | HCID 40067 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-bromo-1-(2H-chromen-3-yl) ethanone | HCID 23007770 | — |
Reaction Steps
3-Acetyl-2H-chromene (0.2 mole) is dissolved in diethyl ether (250 ml) and methanol (10 ml). The solution is cooled to 0°-5° C. Bromine (0.21 mole) is added dropwise thereto, with stirring. The resulting material is left aside 2 hours at room temperature. Anhydrous potassium carbonate (25 g) is then added and the material is evaporated to dryness. The pasty residue is placed in a flask with 600 ml hexane, and is refluxed for 1 hour. The reaction mixture is decanted hot, allowed to cool, and the organic solution is placed in the freezer. Brown-yellow crystals having a sufficient purity for the next step separate out. After two recrystallizations from hexane, a sample gives long pale yellow needles, M.p.=87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04181722 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-a2240ba10c6e4c69a4e2f2fb4c32d6c9 |
| Source note | uspto-grants-1980_01 |