反应 #4120751
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c191c658dad7420aa2266b9522fc8e57暂无可渲染的结构数据
CCOC(=O)NC1=C(C=C(C=C1)Br)F产品信息
乙基 N-(4-溴-2-氟苯基)氨基甲酸酯(CAS 214329-73-4)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
可能的应用方向
仅供专业研发与工业用途
数据库编号 2166334
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c191c658dad7420aa2266b9522fc8e57反应条件: temp:10.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Ethyl chloroformate (15.91 g) was added dropwise to a solution of 4-bromo-2-fluoroaniline (25.33 g) and pyridine (21.06 g) in methylene chloride (260 ml) at 0° C., and the mixture was stirred at 10° C. for 3 hours. After the reaction, it was extracted with methylene chloride, then washed with diluted hydrochloric acid and an aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. Then, methylene chloride was distilled off, and the resulting crude crystals were crystallized from ethyl acetate-n-hexane (1:5 v/v) to obtain the objective ethyl N-(4-bromo-2-fluorophenyl)carbamate (34.45 g). After the reaction, it was extracted with methylene chloride washed with diluted hydrochloric acid an aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate Then, methylene chloride was distilled off the resulting crude crystals were crystallized from ethyl acetate-n-hexane (1:5 v/v)
来源 ID: ord-6b644217c4024409ab2f48ba7aa6c90a反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Ethyl 3-amino-4,4,4-trifluoro-2-methylcrotonate (26.0 g) was dissolved in DMF (123 ml). To this solution, a suspension of sodium methoxide in DNF (7.78 g) was added dropwise at 0° C., and the mixture was stirred at 5° C. for 30 minutes. Then, a DMF solution of ethyl N-(4-bromo-2-fluoro-phenyl)carbamate (31.44 g) was added dropwise thereto, and the mixture was stirred at 130° C. for 5 hours. After the reaction, DMF was distilled off under reduced pressure, and the residue was acidified by adding diluted hydrochloric acid thereto. This was extracted with ethyl acetate, washed with water, and then dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off, and the resulting residue was crystallized from ethyl acetate-n-hexane (1:3 v/v) to obtain the objective 3-(4-bromo-2-fluorophenyl)-5-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione (18.78 g). was added dropwise at 0° C. the mixture was stirred at 130° C. for 5 hours was distilled off under reduced pressure by adding diluted hydrochloric acid This was extracted with ethyl acetate washed with water dried over anhydrous magnesium sulfate Ethyl acetate was distilled off the resulting residue was crystallized from ethyl acetate-n-hexane (1:3 v/v)
来源 ID: ord-97229743c1c04a3ca01a9325971d6085反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c191c658dad7420aa2266b9522fc8e57反应条件: temp:10.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Ethyl chloroformate (15.91 g) was added dropwise to a solution of 4-bromo-2-fluoroaniline (25.33 g) and pyridine (21.06 g) in methylene chloride (260 ml) at 0° C., and the mixture was stirred at 10° C. for 3 hours. After the reaction, it was extracted with methylene chloride, then washed with diluted hydrochloric acid and an aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. Then, methylene chloride was distilled off, and the resulting crude crystals were crystallized from ethyl acetate-n-hexane (1:5 v/v) to obtain the objective ethyl N-(4-bromo-2-fluorophenyl)carbamate (34.45 g). After the reaction, it was extracted with methylene chloride washed with diluted hydrochloric acid an aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate Then, methylene chloride was distilled off the resulting crude crystals were crystallized from ethyl acetate-n-hexane (1:5 v/v)
来源 ID: ord-6b644217c4024409ab2f48ba7aa6c90a反应条件: temp:5.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Ethyl 3-amino-4,4,4-trifluoro-2-methylcrotonate (26.0 g) was dissolved in DMF (123 ml). To this solution, a suspension of sodium methoxide in DNF (7.78 g) was added dropwise at 0° C., and the mixture was stirred at 5° C. for 30 minutes. Then, a DMF solution of ethyl N-(4-bromo-2-fluoro-phenyl)carbamate (31.44 g) was added dropwise thereto, and the mixture was stirred at 130° C. for 5 hours. After the reaction, DMF was distilled off under reduced pressure, and the residue was acidified by adding diluted hydrochloric acid thereto. This was extracted with ethyl acetate, washed with water, and then dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off, and the resulting residue was crystallized from ethyl acetate-n-hexane (1:3 v/v) to obtain the objective 3-(4-bromo-2-fluorophenyl)-5-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione (18.78 g). was added dropwise at 0° C. the mixture was stirred at 130° C. for 5 hours was distilled off under reduced pressure by adding diluted hydrochloric acid This was extracted with ethyl acetate washed with water dried over anhydrous magnesium sulfate Ethyl acetate was distilled off the resulting residue was crystallized from ethyl acetate-n-hexane (1:3 v/v)
来源 ID: ord-97229743c1c04a3ca01a9325971d6085PubChem References
以下资料来自该化合物的公开数据库参考记录。
