HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-Chloro-4-fluoro-5-diacetylaminobenzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Chloro-4-fluoro-5-diacetylaminotoluene | HCID 20032370 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Chloro-4-fluoro-5-diacetylaminobenzyl bromide | HCID 20032367 | 7.9% |
Reaction Steps
A mixture of 7.8 g (0.032 mole) of 2-chloro-4-fluoro-5-diacetylaminotoluene, 6.2 g (0.035 mole) of N-bromosuccinimide, 0.5 g of benzoyl peroxide, and 200 ml of carbon tetrachloride was heated at reflux for two days. This mixture was filtered, and the filtrate was washed with water. The filtrate was dried, and the solvent was evaporated under reduced pressure. The residue was passed through a column of silica gel, eluting with ethyl acetate/heptane (1/4). Appropriate fractions were combined, and the solvent was evaporated under reduced pressure, yielding 0.82 g of 2-chloro-4-fluoro-5-diacetylaminobenzyl bromide. The nmr was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04846882 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-af7bd7184ea249b885311bb03f4c861a |
| Source note | uspto-grants-1989_07 |