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) benzylbromide in 450 mL acetonitrile was refluxed for 3 h, cooled to RT and evaporated down i.vac. The residue was combined with EtOAc, the organic phase was washed with water and saturated NaCl solution, dried over Na2SO4 and evaporated down i.vac.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696209B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-7ed29cdc0eda4984ad8d2aeb9fbd574b |
| Source note | uspto-grants-2010_04 |