HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → [4-(1-Bromoethyl)phenyl](thiophen-2-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Ethylphenyl 2-thienyl ketone | HCID 104321 | — |
| Catalyst | Toluene | HCID 1140 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | [4-(1-Bromoethyl)phenyl](thiophen-2-yl)methanone | HCID 103685 | — |
Reaction Steps
A mixture of 23.5 parts of p-ethylphenyl 2-thienyl ketone, 19.5 parts of N-bromosuccinimide, 220 parts of carbon tetrachloride, 1.1 parts of benzoyl peroxide and one drop of toluene is stirred and refluxed for 2 hours. The precipitated succinimide is filtered off and the carbon tetrachloride filtrate is dried and evaporated. The oily residue solidifies on cooling. The solid product is dissolved in 2-propanol and the product is allowed to crystallize. It is filtered off and dried in vacuo, yielding α-bromo-α-methyl-p-tolyl 2-thienyl ketone; mp. 71.1° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04035376 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-de0992edeaa14a218cdd4f2ab40b388b |
| Source note | uspto-grants-1977_07 |