HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromobenzene → 1-(2-Bromophenyl)pentan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Pentanoic Acid | HCID 7991 | — |
| Reactant | Chloroacetic anhydride | HCID 10946 | — |
| Solvent | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| Product | 1-(2-Bromophenyl)pentan-1-one | HCID 12158127 | 56% |
Reaction Conditions
| Temperature | 115 °C |
|---|
Reaction Steps
In 50 ml of tetrachloroethane were dissolved 5.11 g (0.05 mole) of valeric acid and 9.83 g (0.0575 mole) of monochloroacetic anhydride. To the resulting solution were added 9.42 g (0.06 mole) of bromobenzene and 0.8 g of boron trifluoride-diethyl ether complex and the resulting mixture was then stirred at 115° C. for 10 hours. After completion of the reaction, the reaction solution was cooled and washed successively with water, 5% aqueous sodium carbonate solution and water. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain 6.75 g of valerylbromobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05235068 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-5a061d4b7f914d01b512268cec9d6b76 |
| Source note | uspto-grants-1993_08 |