HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 2-Bromoindenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1-Indanone | HCID 6735 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Bromoindenone | HCID 9990649 | — |
Reaction Steps
The indanone compound of formula 6 prepared in Step 3, NBS (2 to 3 eq), and AIBN (1 to 0.2 eq) are dissolved in CCl4. Then, the mixture is allowed to reflux for 30 min to 1 h with stirring and then is further irradiated by a tungsten lamp (375 W) for 1 to 2 h with stirring, to obtain the 2-bromo-1H-indenone of formula 7. In other way, the mixture may be allowed to reflux for 2 to 9 h with stirring while being irradiated by a tungsten lamp (375 W), to obtain the 2-bromo-1H-indenone of formula 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877747B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-06f01594d913490e8c64c4147c6cb722 |
| Source note | uspto-grants-2014_11 |