HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 7-BROMO-2,3-DIMETHYL-1-BENZOFURAN
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 15381110 | HCID 15381110 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 7-BROMO-2,3-DIMETHYL-1-BENZOFURAN | HCID 11096262 | 91.4% |
Reaction Steps
25 ml of concentrated sulphuric acid are introduced into a 100 ml three-necked flask equipped with a thermometer and a 10 ml dropping funnel and cooling is carried out to between -15 and 0° C. with a bath of solid carbon dioxide in acetone. 3-(2-Bromophenoxy)-2-butanone (5 g, 20.6 mmol) is added dropwise and stirring is continued for 5 min. The mixture is poured onto crushed ice and then extraction is carried out with ethyl acetate (3×80 ml). The organic phases are combined, dried over magnesium sulphate and concentrated. The residue is purified by silica column chromatography (elution solvent: cyclohexane). 4.24 g (Yield: 91%) of 2,3-dimethyl-7-bromobenzofuran are obtained--M.p.: 33° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063810 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-3967f8d9b6504b879c696d25a1cd0ce8 |
| Source note | uspto-grants-2000_05 |