HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → HCID 68428806, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 4-Methyl-2-(3-methoxyphenyl)thiazole-5-carboxylate | HCID 50997800 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 68428806 | HCID 68428806 | 94.4% |
Reaction Steps
A mixture of 2-(3-methoxy-phenyl)-4-methyl-thiazole-5-carboxylic acid ethyl ester (3.01 g, 10.88 mmole), N-bromosuccinimide (2.03 g, 11.42 mole) and benzoyl peroxide (132 mg, 0.54 mmole) in carbon tetrachloride (40 ml) was refluxed for 16 h before it was cooled to room temperature and partitioned between dichloromethane and water. The organic layer was washed with saturated aqueous sodium bicarbonate solution, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give the title compound as a yellow solid (3.66 g). MS: (+) m/z 355.92, 357.92 (M+1, 79Br/81Br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696223B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-64e1479529ce4069bfd5fff726a5dea3 |
| Source note | uspto-grants-2010_04 |