HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 4-(2-Methoxyphenyl)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methoxy-4'-methyl-1,1'-biphenyl | HCID 10313541 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(2-Methoxyphenyl)benzyl bromide | HCID 21904136 | — |
Reaction Steps
2-methoxy-4′-methylbiphenyl, 160 mg (0.81 mmol), NBS, 158 mg (0.91 mmol), and AIBN, 1 mg (0.006 mmol) were suspended in 7 mL tetrachloromethane, and refluxed for 24 hours. The product was filtered, and the solvent removed from the filtrate by rotary evaporation. Equal amounts of diethyl ether and water were added and the product extracted. The ether layer was separated and dried over MgSO4, filtered, and the solvent removed. 4-(2-Methoxyphenyl)benzyl bromide, 128 mg, was obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192918B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-d5ec89be604148009bd67110a711d7e4 |
| Source note | uspto-grants-2007_03 |