HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 67125220, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 4-(2-chlorophenyl)-2-methylpyrimidine-5-carboxylate | HCID 18981952 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 67125220 | HCID 67125220 | — |
Reaction Steps
820 mg (2.96 mmol) of ethyl 4-(2-chlorophenyl)-2-methylpyrimidine-5-carboxylate and 633 mg (3.55 mmol) of N-bromosuccinimide were dissolved in 18 ml of carbon tetrachloride and, with stirring, heated to the boil. At boiling point, 49 mg (0.29 mmol) of 2,2′-azobis-2-methylpropionitrile were added a little at a time over a period of 5 hours, followed by refluxing for a further hour. After cooling to room temperature, the reaction solution was filtered and the mother liquor was freed from the solvent under reduced pressure. The desired product was isolated by chromatographic purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08980886B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-f560c7d869f14d1fb147ae7209bc58bf |
| Source note | uspto-grants-2015_03 |