HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Bromo-6-Chloro-Phthalide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Chloro-3H-isobenzofuran-1-one | HCID 7174165 | — |
| Reactant | Azobisbutyronitrile | HCID 14151322 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Bromo-6-Chloro-Phthalide | HCID 12298538 | — |
Reaction Steps
6-Chlorophthalide (7.66 gms; 0.0452 mole), N-bromosuccinimide (8.1 gms; 0.0452 mole) and azobisbutyronitrile (0.1 gm) were gently refluxed in dry carbon tetrachloride (150 ml.) for 11/2 hours. On cooling, the succinimide was filtered off and the solvent removed in vacuo to leave a yellow solid, which was used immediately. Yield 9.57 gms. 86.2%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04036829 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-f756589f3d0541b297d5073c29ad0be3 |
| Source note | uspto-grants-1977_07 |