HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dibromobenzene → 2-Bromo-1-(2,4-dibromophenyl)-1-propanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Propanoyl bromide, 2-bromo- | HCID 79047 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 2-Bromo-1-(2,4-dibromophenyl)-1-propanone | HCID 18967754 | 76% |
Reaction Steps
15 g of aluminium chloride are added with caution, at 0° C., to 25 g of 1,3-dibromobenzene in 250 ml of carbon disulphide, and 22.86 g of 2-bromopropionyl bromide are then run in slowly. The mixture is maintained at reflux for 8 hours, then the carbon disulphide is evaporated off under vacuum and the reaction medium is poured onto crushed ice. The product is extracted twice with heptane, dried, evaporated to dryness and then purified on a column of silica, using a mixture of cyclohexane and ethyl acetate (10:1 v/v) as eluent, to give the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05602132 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-3e2bbc48b6d24aafa22a7efc9850e394 |
| Source note | uspto-grants-1997_02 |