Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 59187446 | HCID 59187446 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59187443 | HCID 59187443 | — |
Reaction Steps
N-Bromosuccinimide (344 mg, 1.61 mmol) is added to a solution of 5-(2-chlorophenyl)-2-methylthiazole (337 mg, 1.93 mmol) in carbon tetrachloride (15 mL). The above solution is stirred at 75° C. for 18 h. The solution is diluted with CH2Cl2 (50 mL) and washed with saturated NaHCO3 (50 mL) and brine (30 mL). The organic layer is dried (MgSO4), filtered, concentrated and purified by silica gel chromatography (EtOAc/hexane, gradient) to give 2-(bromomethyl)-5-(2-chlorophenyl)thiazole 7 as a white solid. MS calcd. for C10H8BrClNS (M+H+) 287.9. found 286.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394841B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-1e2abb98b6f9457e8c44793136e290e9 |
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| Source note | uspto-grants-2013_03 |
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