HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-(5-Bromomethyl-thiazol-4-yl)-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-(5-Methyl-thiazol-4-yl)-benzoic acid methyl ester | HCID 69689272 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(5-Bromomethyl-thiazol-4-yl)-benzoic acid methyl ester | HCID 69687702 | 104.6% |
Reaction Steps
A mixture of 3-(5-methyl-thiazol-4-yl)-benzoic acid methyl ester (2.40 g), N-bromosuccinimid (2.01 g) and α,α′-bis(isobutyronitrile) (0.02 g) in CCl4 (40 mL) was heated at reflux for 30 min. The cooled mixture was filtered and the solvent was evaporated to give crude 3-(5-bromomethyl-thiazol-4-yl)-benzoic acid methyl ester (3.36 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06544985B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-c17ef2d957ae41fcace9579ab5b3c222 |
| Source note | uspto-grants-2003_04 |