HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 3-Bromomethyl-5-chloro-2-phenylbenzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Chloro-3-methyl-2-phenyl-1-benzothiophene | HCID 821982 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Bromomethyl-5-chloro-2-phenylbenzo[b]thiophene | HCID 21916774 | — |
Reaction Steps
In a 100 ml round-bottomed flask, 1 eq. of the compound obtained in Step B is dissolved in 20 ml of CCl4. 1 eq. of N-bromosuccinimide and 0.04 eq. of benzoyl peroxide are then added, and the mixture is irradiated by means of a halogen lamp and maintained at reflux for 4 hours. At the end of the reaction, the insoluble material is filtered off, and the carbon tetrachloride is evaporated off. The residue obtained is purified by chromatography on a silica gel column.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872851B1 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-2e4ca7c5a58e4dc3b50567ecb43d6a3d |
| Source note | uspto-grants-2005_03 |