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 | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-2-ethyl-6-methyl-1-benzyloxybenzene | HCID 22006813 | 97% |
Reaction Steps
To a mixture of 26 g of 4-bromo-2-ethyl-6-methylphenol, 24.8 g of benzyl bromide and 200 ml of N,N-dimethylformamide was added 21.7 g of potassium carbonate, while stirring at room temperature. After stirring at room temperature for 24 hours, the reaction mixture was poured into ice water, and extracted twice with 500 ml of diethyl ether. The diethyl ether layers were combined, washed with water, dried over anhydrous magnesium sulfate, and then concentrated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 35.6 g of 4-bromo-2-ethyl-6-methyl-1-benzyloxybenzene (97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06214835B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-37dbb46dddc04e7aa80bf91a2014ba12 |
| Source note | uspto-grants-2001_04 |