HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-(Bromomethyl)-1-methoxy-3-methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,3-Dimethylanisole | HCID 76269 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(Bromomethyl)-1-methoxy-3-methylbenzene | HCID 10353222 | — |
Reaction Steps
0.50 g (3.68 mmol) of 2,3-dimethylanisole was dissolve in 10 ml of carbon tetrachloride. The resultant solution was then added with 0.72 g (4.04 mmol) of N-bromosuccinimide, and the obtained solution was subjected to irradiation of light (Infrared lamp 375WR manufactured by Toshiba) for 45 min. at the reflux temperature. The solution was then cooled down, and the temperature thereof was maintained at a room temperature to cause the precipitation. The precipitated succinimide was separated by filtration, and the obtained filtrate was condensed under reduced pressure to produce a crude product of 2-methoxy-6-methylbenzyl bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06589967B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-b21b8281ce6f44fd99f17c0ceed44602 |
| Source note | uspto-grants-2003_07 |