| Identification | Back Directory | [Name]
5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER | [CAS]
954239-61-3 | [Synonyms]
Methyl 5-broMobenzo[d]oxazole-2-carboxylate 5-Bromo-2-benzoxazolecarboxylic acid methyl ester 5-bromo-benzoxazole-2-carboxylic acid methyl ester 5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER 2-Benzoxazolecarboxylic acid, 5-bromo-, methyl ester | [Molecular Formula]
C9H6BrNO3 | [MDL Number]
MFCD09832200 | [MOL File]
954239-61-3.mol | [Molecular Weight]
256.05 |
| Hazard Information | Back Directory | [Synthesis]
Catalyst (9.9 mg, 0.025 mmol, 5 mol%), potassium tert-butoxide (0.0672 g, 0.6 mmol), DMF (3.0 mL) and 5-bromobenzoxazole (99.01 mg, 0.5 mmol) were added to the reaction flask under argon protection. The reaction mixture was stirred at 80 °C for 18 h under carbon dioxide atmosphere at atmospheric pressure. Upon completion of the reaction, the system was cooled to 65 °C, followed by the addition of iodomethane (93 μL, 1.5 mmol) and continued stirring at 65 °C for 1 hour. At the end of the reaction, the mixture was cooled to room temperature and the reaction was quenched with deionized water. The reaction mixture was extracted with ethyl acetate, and the organic phases were combined and purified by column chromatography (eluent: ethyl acetate/petroleum ether, 1:10, v/v). The target product methyl 5-bromobenzo[D]oxazole-2-carboxylate was obtained in 85% yield. | [References]
[1] Green Chemistry, 2018, vol. 20, # 5, p. 989 - 996 [2] Patent: CN106565623, 2017, A. Location in patent: Paragraph 0035 |
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