HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chlorobiphenyl → 1-Bromo-2-(3'-chlorobiphenyl-4-yl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chlorobiphenyl | HCID 16322 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Bromo-2-(3'-chlorobiphenyl-4-yl)ethanone | HCID 22335475 | 55.9% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
A mixture of 5 g (0.026 mole) of 3-chlorobiphenyl, 50 ml of methylene chloride, 6.95 g (0.034 mole) of bromoacetyl bromide is cooled to 0–5° C. and 4 g (0.030 mole) of aluminum trichloride are added. The mixture is stirred for 1 hour at 5° C., then for 4 hours at room temperature. It is poured onto an ice/water mixture, extracted with methylene chloride, the organic phase is washed with a 1N solution of HCl, dried over sodium sulfate and evaporated under reduced pressure. 4.5 g of the title product is obtained. M.p. 63–65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07151107B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-76dd2cbff254438d831413e088177cb4 |
| Source note | uspto-grants-2006_12 |