HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 67125229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 86660450 | HCID 86660450 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 67125229 | HCID 67125229 | — |
Reaction Steps
5.00 g (18.6 mmol) of methyl 4-(2-chlorophenyl)-2-methyl-1,3-thiazole-5-carboxylate and 3.38 g (19.0 mmol) of N-bromosuccinimide were dissolved in 100 ml of carbon tetrachloride and, with stirring, heated to the boil. At boiling point, 170 mg (1.00 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-21533b6f4c734816b9b2ab9a4f777c94 |
| Source note | uspto-grants-2015_03 |