HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 14365629, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 56984503 | HCID 56984503 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 14365629 | HCID 14365629 | — |
Reaction Steps
10 g (33.8 mmol) of 9-acetyl-4-methyl-β-carboline-3carboxylic acid ethyl ester is combined in 500 ml of carbon tetrachloride with 12 g (67.4 mmol) of N-bromosuccinimide and one spatula tip of azobisisobutyronitril and heated to reflux for 1.5 hours while simultaneously exposing the reaction mixture to light. After cooling, the mixture is suctioned off from the succinimide, concentrated, and the residue is extracted by stirring with hot water and suctioned off. Yield: 10.64 g (84%) of 9-acetyl-4-bromomethyl-β-carboline-β-carboxylic acid ethyl ester, mp 188°-189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04945163 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-b4bd2254a5dc47508b704470f3d5ff74 |
| Source note | uspto-grants-1990_07 |