HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-5-methyl-3-phenylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-Methyl-3-phenylbenzofuran | HCID 3835920 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-5-methyl-3-phenylbenzofuran | HCID 21330922 | — |
Reaction Steps
To a solution of 119 g (0.816 mole) of 5-methyl-3-phenylbenzofuran in 1 l. of chloroform at 20° to 25° C. is added 143.5 g (0.895 mole) of bromine. The mixture is evaporated under vacuum and the residue is dissolved in diethyl ether. The ether solution is washed with water, 10% sodium bicarbonate solution and saturated sodium chloride solution. The dried mixture is filtered and the filtrate is evaporated under vacuum. The residue is suspended in hot petroleum ether, then the mixture is cooled to provide solid 2-bromo-5-methyl-3-phenylbenzofuran, m.p. 52°-57° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04141990 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-b752784358c14f7eae27ce46317ae509 |
| Source note | uspto-grants-1979_02 |