反应 #4137420
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-123063442d854b70bb3cd5e029207fb4暂无可渲染的结构数据
C1=C(C=C(C(=C1OC(F)(F)F)N)Cl)Br产品信息
4-溴-2-氯-6-(三氟甲氧基)苯胺(CAS 885266-98-8)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 17750065
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
7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-123063442d854b70bb3cd5e029207fb4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-123063442d854b70bb3cd5e029207fb4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-123063442d854b70bb3cd5e029207fb4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-bromo-2-chloro-6-trifluoromethoxy-aniline (2.9 g, 10 mmol) and triethylamine (1.5 g, 15 mmol) in anhydrous dichloromethane (50 mL) was added dropwise tert-butylacetyl chloride (1.6 g, 12 mmol) with stirring at room temperature. The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture was diluted with dichloromethane and washed with water and dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min) to give a white solid (3.6 g, 93%). The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture washed with water dried over anhydrous sodium sulfate evaporated to dryness under reduced pressure The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min)
来源 ID: ord-433a9f37a1134e9887ceeb673a4c0f8f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-bromo-2-chloro-6-trifluoromethoxy-aniline (2.9 g, 10 mmol) and triethylamine (1.5 g, 15 mmol) in anhydrous dichloromethane (50 mL) was added dropwise tert-butylacetyl chloride (1.6 g, 12 mmol) with stirring at room temperature. The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture was diluted with dichloromethane and washed with water and dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min) to give a white solid (3.6 g, 93%). The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture washed with water dried over anhydrous sodium sulfate evaporated to dryness under reduced pressure The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min)
来源 ID: ord-433a9f37a1134e9887ceeb673a4c0f8f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-bromo-2-chloro-6-trifluoromethoxy-aniline (2.9 g, 10 mmol) and triethylamine (1.5 g, 15 mmol) in anhydrous dichloromethane (50 mL) was added dropwise tert-butylacetyl chloride (1.6 g, 12 mmol) with stirring at room temperature. The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture was diluted with dichloromethane and washed with water and dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min) to give a white solid (3.6 g, 93%). The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture washed with water dried over anhydrous sodium sulfate evaporated to dryness under reduced pressure The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min)
来源 ID: ord-aab51d2c09ce4305ae20db474c40ebe8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-bromo-2-chloro-6-trifluoromethoxy-aniline (2.9 g, 10 mmol) and triethylamine (1.5 g, 15 mmol) in anhydrous dichloromethane (50 mL) was added dropwise tert-butylacetyl chloride (1.6 g, 12 mmol) with stirring at room temperature. The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture was diluted with dichloromethane and washed with water and dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min) to give a white solid (3.6 g, 93%). The reaction mixture was stirred for 3 hours at room temperature, than the reaction mixture washed with water dried over anhydrous sodium sulfate evaporated to dryness under reduced pressure The residue was purified by silica gel column (ISCO, hexane/EtOAc, 0-40%, 40 min)
来源 ID: ord-433a9f37a1134e9887ceeb673a4c0f8fPubChem References
以下资料来自该化合物的公开数据库参考记录。
