反应 #4138000
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-f6ee94b8074a4194a9a721e00c35f97a暂无可渲染的结构数据
C1=CC=C(C=C1)COC(=O)NCC2=CC=C(C=C2)N产品信息
4-N-CBZ-氨基甲基苯胺(CAS 168050-39-3)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。
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9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f6ee94b8074a4194a9a721e00c35f97a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f433258312fc49afb0437a9c97256099反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f6ee94b8074a4194a9a721e00c35f97a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f6ee94b8074a4194a9a721e00c35f97a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-aminobenzenemethanamine (1.5 g, 12.3 mmol) in 20 mL CH2Cl2 was added benzylchloroformate (1.57 mL, 11 mmol), followed by triethylamine (Et3N) (1.5 mL, 11 mmol) at room temperature. White percipitates was observed immediately. The reaction was stirred at room temperature for 10 minutes and removed Et3N salt by filtration. The reaction mixture was concentrated in vacuo and partitioned between EtOAc and H2O. The EtOAc layer was washed with a sat. solution of KHSO4, a sat. solution of NaHCO3, concentrated in vacuo and subjected to a silica-gel column using CHCl3 /CH3OH=25/1 ratio as an eluting solvent to give title compound (43% yield). removed Et3N salt by filtration The reaction mixture was concentrated in vacuo partitioned between EtOAc and H2O The EtOAc layer was washed with a sat. solution of KHSO4 a sat. solution of NaHCO3, concentrated in vacuo
来源 ID: ord-018e39b62ef0400799923e40ee9b38f4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f433258312fc49afb0437a9c97256099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-aminobenzenemethanamine (1.5 g, 12.3 mmol) in 20 mL CH2Cl2 was added benzylchloroformate (1.57 mL, 11 mmol), followed by triethylamine (Et3N) (1.5 mL, 11 mmol) at room temperature. White percipitates was observed immediately. The reaction was stirred at room temperature for 10 minutes and removed Et3N salt by filtration. The reaction mixture was concentrated in vacuo and partitioned between EtOAc and H2O. The EtOAc layer was washed with a sat. solution of KHSO4, a sat. solution of NaHCO3, concentrated in vacuo and subjected to a silica-gel column using CHCl3 /CH3 OH=25/1 ratio as an eluting solvent to give title compound (43% yield). removed Et3N salt by filtration The reaction mixture was concentrated in vacuo partitioned between EtOAc and H2O The EtOAc layer was washed with a sat. solution of KHSO4 a sat. solution of NaHCO3, concentrated in vacuo
来源 ID: ord-70c92724924f40e9aff39668dc762cfb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-aminobenzenemethanamine (1.5 g, 12.3 mmol) in 20 mL CH2Cl2 was added benzylchloroformate (1.57 mL, 11 mmol), followed by triethylamine (Et3N) (1.5 mL, 11 mmol) at room temperature. White percipitates was observed immediately. The reaction was stirred at room temperature for 10 minutes and removed Et3N salt by filtration. The reaction mixture was concentrated in vacuo and partitioned between EtOAc and H2O. The EtOAc layer was washed with a sat. solution of KHSO4, a sat. solution of NaHCO3, concentrated in vacuo and subjected to a silica-gel column using CHCl3 /CH3 OH=25/1 ratio as an eluting solvent to give title compound (43% yield). removed Et3N salt by filtration The reaction mixture was concentrated in vacuo partitioned between EtOAc and H2O The EtOAc layer was washed with a sat. solution of KHSO4 a sat. solution of NaHCO3, concentrated in vacuo
来源 ID: ord-fd824cede41e404cbd65edc940e9af7e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-aminobenzenemethanamine (1.5 g, 12.3 mmol) in 20 mL CH2Cl2 was added benzylchloroformate (1.57 mL, 11 mmol), followed by triethylamine (Et3N) (1.5 mL, 11 mmol) at room temperature. White percipitates was observed immediately. The reaction was stirred at room temperature for 10 minutes and removed Et3N salt by filtration. The reaction mixture was concentrated in vacuo and partitioned between EtOAc and H2O. The EtOAc layer was washed with a sat. solution of KHSO4, a sat. solution of NaHCO3, concentrated in vacuo and subjected to a silica-gel column using CHCl3 /CH3OH=25/1 ratio as an eluting solvent to give title compound (43% yield). removed Et3N salt by filtration The reaction mixture was concentrated in vacuo partitioned between EtOAc and H2O The EtOAc layer was washed with a sat. solution of KHSO4 a sat. solution of NaHCO3, concentrated in vacuo
来源 ID: ord-018e39b62ef0400799923e40ee9b38f4PubChem References
以下资料来自该化合物的公开数据库参考记录。
