HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isophorone → 4-Bromo-3,5,5-trimethylcyclohex-2-en-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isophorone | HCID 6544 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-Bromo-3,5,5-trimethylcyclohex-2-en-1-one | HCID 12794064 | — |
Reaction Steps
A mixture of isophorone (13.82 g; 0.1 Mole) and N-bromo-succinimide (17.80 g; 0.1 Mole) in the presence of traces of α,α'-azodiisobutyronitrile was refluxed in 500 ml of CCl4 during 15 minutes. 500 ml of petrol-ether (30°-50° C.) were then added to the cool reaction mixture and the succinimide thus precipitated was filtered off. By evaporating the volatile components of the clear filtrate, crude 3,5,5-trimethyl-4-bromo-cyclohex-2-en-1-one was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04031902 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-b1c00807aeb14629a08cb87a1f1404b8 |
| Source note | uspto-grants-1977_06 |