HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromobenzene → HCID 22504545, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 22504616 | HCID 22504616 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22504545 | HCID 22504545 | — |
Reaction Steps
4-Benzyloxy-2-(4-chlorophenyl)-1-[4-(2-dimethylaminoethoxy)phenyl]butan-1-one (9.4 g, 0.021 mol) is added to Grignard reagent prepared from bromobenzene (13.1 g, 0.083 mol) and Mg turnings (2.0 g, 0.083 mol) in dry tetrahydrofuran. The mixture is refluxed for 3 h. Saturated ammonium chloride solution is added to the cooled reaction mixture, the THF layer is separated and the aqueous phase is extracted with toluene. The combined organic phases are washed with water and the solvents are evaporated. The residual product (10.7 g) is used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06576645B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-847584165ed346478c10fd9209aae608 |
| Source note | uspto-grants-2003_06 |