HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 4-Bromo-2-methyl-1-(phenylmethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-methylphenol | HCID 16896 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-2-methyl-1-(phenylmethoxy)benzene | HCID 22636847 | 89.3% |
Reaction Steps
To 4-bromo-2-methylphenol (1.25 g, 6.67 mmol) in 20 ml MeCN were added dry K2CO3 (1.84 g, 13.34 mmol, 2 equiv) and benzylbromide (0.872 ml, 7.34 mmol, 1.1 equiv) and reaction is stirred for 24 h at room temperature. Reaction mixture was filtered through Celite, solution was concentrated and purified by silica gel column chromatography (Hexane to 8% EtOAc/Hexane) to give 1.65 g 17 in 89% yield. Rf=0.90 (20% EtOAc/Hexane);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428447B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-ea427bd705c84ba29d74b3749fe28e82 |
| Source note | uspto-grants-2016_08 |