HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 1(3H)-Isobenzofuranone, 3-bromo-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Phthalide | HCID 6885 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1(3H)-Isobenzofuranone, 3-bromo- | HCID 96218 | — |
Reaction Steps
1H-Isobenzofuran-3-one (40.2 g, 0.3 moles), N-bromosuccinimide (53.4 g., 0.03 moles) and azo-bisisobutyronitrile (1g) were combined in 500 mL of CCl4 and refluxed under nitrogen for 2 hours. The reaction mixture was cooled to room temperature, filtered and the filtrate concentrated in vacuo to a solid residue. The latter was crystallized from cyclohexane to yield title product, 34.5 g., m.p. 78°-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04536393 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-94c8bc63d9594a6e86e79edf6d413015 |
| Source note | uspto-grants-1985_08 |