HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-Bromo-2-ethyl-6-methyl-1-benzyloxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-ethyl-6-methylphenol | HCID 22006838 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-2-ethyl-6-methyl-1-benzyloxybenzene | HCID 22006813 | — |
Reaction Steps
A suspension of 39.8 g (185 mmol) 4-bromo-2-ethyl-6-methyl-phenol, 63.9 g (0.46 mmol) K2CO3 and 22.0 mL (185 mmol) benzyl bromide in 450 mL acetonitrile was refluxed for 3 h, cooled to RT and concentrated by evaporation i. vac. The residue was combined with EtOAc, the organic phase was washed with water and saturated NaCl solution, dried on Na2SO4 and concentrated by evaporation i. vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582625B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-760f3dae8aef4473948faaf95e702195 |
| Source note | uspto-grants-2009_09 |