反应 #4121728
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-11134ddbfba6417b95ade23c2e4ee8f5暂无可渲染的结构数据
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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-11134ddbfba6417b95ade23c2e4ee8f5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b992b61d03bc4f9b91da16ec3f9db330反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In a manner similar to Preparation 1, react 1-iodobutane with 3-piperidinone to obtain the title compound. In a manner similar to Preparation 1
来源 ID: ord-d982e50d1e9146b4bdddcc8ddf3b77a3反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 3-piperidone (12 mmol) in 200 mL of methylene chloride. is added triethylamine (18 mmol) in a single portion at room temperature and the reaction mixture cooled to 0° C. Benzyl chloroformate (12 mmol) is added dropwise via addition funnel and the reaction mixture allowed to warm to room temperature. Stirring is continued for 2 hours at room temperature. The reaction mixture is diluted with ethyl acetate (200 mL) and washed with 1N hydrochloric acid (3×100 mL), water and brine. The organic layer is worked up to provide N-Benzyloxycarbonyl-3-piperidone. to warm to room temperature washed with 1N hydrochloric acid (3×100 mL), water and brine
来源 ID: ord-b80596e8795847d2a8083ccfffd02bdf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In a manner similar to Preparation 1, react 1-iodobutane with 3-piperidinone to obtain the title compound. In a manner similar to Preparation 1
来源 ID: ord-d982e50d1e9146b4bdddcc8ddf3b77a3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-11134ddbfba6417b95ade23c2e4ee8f5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b992b61d03bc4f9b91da16ec3f9db330反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 3-piperidone (12 mmol) in 200 mL of methylene chloride. is added triethylamine (18 mmol) in a single portion at room temperature and the reaction mixture cooled to 0° C. Benzyl chloroformate (12 mmol) is added dropwise via addition funnel and the reaction mixture allowed to warm to room temperature. Stirring is continued for 2 hours at room temperature. The reaction mixture is diluted with ethyl acetate (200 mL) and washed with 1N hydrochloric acid (3×100 mL), water and brine. The organic layer is worked up to provide N-Benzyloxycarbonyl-3-piperidone. to warm to room temperature washed with 1N hydrochloric acid (3×100 mL), water and brine
来源 ID: ord-b80596e8795847d2a8083ccfffd02bdf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In a manner similar to Preparation 1, react 1-iodobutane with 3-piperidinone to obtain the title compound. In a manner similar to Preparation 1
来源 ID: ord-d982e50d1e9146b4bdddcc8ddf3b77a3