HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 5-Bromo-3,3-dimethylbenzofuran-2(3H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2(3H)-Benzofuranone, 3,3-dimethyl- | HCID 595620 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 5-Bromo-3,3-dimethylbenzofuran-2(3H)-one | HCID 16220634 | — |
Reaction Steps
2,3-Dihydro-3,3-dimethylbenzofuran-2-one (1.62 g, 0.01 mole), in carbon tetrachloride (25 ml) containing catalytic amounts of iron filings and iodine was treated with bromine (1.6 g, 0.01 mole) and the mixture boiled under reflux for 1 hour. The solvent was removed under vacuum and the residue taken up in petroleum ether (b.p. 60°-80° C.). The solution was decanted from a little insoluble residue and washed with aqueous sodium metabisulphite and water, dried over magnesium sulphate and run down. The title product was obtained as a white solid m.p. 49°-53° C. and was shown by NMR to be a slightly impure sample of the product obtained in Example 3(b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04333759 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-08b44c19d50a487ba35eaa88d01d0b12 |
| Source note | uspto-grants-1982_06 |