Basic information Safety Supplier Related

5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER

Basic information Safety Supplier Related

5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Basic information

Product Name:
5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER
Synonyms:
  • 5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER
  • 2-Benzoxazolecarboxylic acid, 5-bromo-, methyl ester
  • Methyl 5-broMobenzo[d]oxazole-2-carboxylate
  • 5-Bromo-2-benzoxazolecarboxylic acid methyl ester
  • 5-bromo-benzoxazole-2-carboxylic acid methyl ester
  • Methyl 5-Bromobenzoxazole-2-carboxylate
  • methyl 5-bromo-1,3-benzoxazole-2-carboxylate
CAS:
954239-61-3
MF:
C9H6BrNO3
MW:
256.05
Mol File:
954239-61-3.mol
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5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
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5-BROMO-BENZOOXAZOLE-2-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis

Synthesis

132244-31-6

124-38-9

74-88-4

954239-61-3

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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