HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-(Bromomethyl)-2-chlorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Chloro-5-methylbenzonitrile | HCID 12557200 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-(Bromomethyl)-2-chlorobenzonitrile | HCID 14033035 | 30.4% |
Reaction Steps
A mixture of 2-chloro-5-methylbenzonitrile (10.6 g, 69.9 mmol), N-bromosuccinimide (12.2 g, 68.5 mmol), and dibenzoyl peroxide (349 mg, 1.44 mmol) in benzene (350 ml) was refluxed 1.5 hours, cooled, and evaporated to dryness under vacuum. The residue was suspended in 7:3 (v/v) hexane-dichloromethane, filtered, and evaporated. The crude product was chromatographed on silica gel (650 g) eluted with 7:3 (v/v) hexane-dichloromethane to provide 4.8 g (30%) 4-chloro-3-cyanobenzyl bromide, m.p. 55°-58° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04816469 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-df76d66bf66e4a0f825f92a8343fa05c |
| Source note | uspto-grants-1989_03 |