HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 1-(Bromomethyl)-2-chloro-3-methylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 1-Chloro-2,6-dimethylbenzene | HCID 32885 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-(Bromomethyl)-2-chloro-3-methylbenzene | HCID 15364466 | — |
Reaction Steps
A solution of 2-chloro-m-xylene (5.00 g, 35.60 mmol), NBS (5.70 g, 32.03 mmol), and a catalytic amount of benzoyl peroxide (100 mg) in CCl4 was refluxed for 1 hour. After cooling to room temperature the resulting mixture was filtered and the filtrate was distilled off. Purification by column chromatography using pentane as the eluant followed by distillation afforded the title compound. Spectroscopic data: 1H NMR (300 MHz, CDCl3.) δ 2.39 (s, 3H), 4.61 (s, 2H), 7.08-7.23 (m, 2H), 7.25-7.30 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557853B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-e569125c88214a4ab8e24fa7f3a77c0e |
| Source note | uspto-grants-2013_10 |