HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → N-[6-(Bromomethyl)pyridin-2-yl]-2,2-dimethylpropanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | N-(6-Methylpyridin-2-yl)pivalamide | HCID 3251458 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | N-[6-(Bromomethyl)pyridin-2-yl]-2,2-dimethylpropanamide | HCID 14326706 | 5% |
Reaction Steps
2,2 ethyl-N-(6-methyl-2-pyridinyl)propaneamide (21-1) (32 g) and N-bromosuccinimide (29.6 g) were added to carbon tetrachloride (300 ml) and to the mixture was added AIBN (15 mg), followed by reluxing for 20 hours under light emitted by 500 W lamp. The resulting mixture was cooled to room temperature, filtered, and concentrated under reduced pressure. The residue was purified by column-chromatography (hexane/ethyl acetate=10/1) to yield the compound 21-2 (1.94 g, 5%) as a pure white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071650B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-992db61ff61e4a0290ab8a231e1f7778 |
| Source note | uspto-grants-2011_12 |