HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-(Bromomethyl)-3-methoxybenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Methoxy-4-methylbenzonitrile | HCID 14752994 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Catalyst | Tungsten | HCID 23964 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(Bromomethyl)-3-methoxybenzonitrile | HCID 14752995 | 65% |
Reaction Steps
N-Bromosuccinimide (3.2 g.) and benzoyl peroxide (0.005 g.) were added to a solution of 3-methoxy-4-methylbenzonitrile (2.65 g.) in dry carbon tetrachloride (90 ml.). The mixture was heated to reflux for 15 minutes using a 250 watt tungsten lamp. The cooled reaction mixture was diluted with petrolum ether (b.p. 60°-80° C., 90 ml.), insoluble material removed by filtration, and the filtrate evaporated. The solid residue was recrystallized from a mixture of dichloromethane and petroleum ether to give 4-bromomethyl-3-methoxybenzonitrile (W) (2.64 g., 65%) as a white solid, m.p. 87°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05030643 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-bf0a5a5d1fc647c5824c427e22b8c39f |
| Source note | uspto-grants-1991_07 |