反应 #4081650
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-df10238793684e25a82a19da1f7d9d09暂无可渲染的结构数据
C=CC(=O)N1CCCCC1产品信息
1-(哌啶-1-基)丙-2-烯-1-酮(CAS 10043-37-5)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-df10238793684e25a82a19da1f7d9d09反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in 50 ml of CH2Cl2 was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, it was furthered dried to a clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a H2O bath at 60° C. without vacuum Once most solvent had been evaporated off it was furthered dried to a clear oil under high vacuum at RT for 30 min.
来源 ID: ord-454d7df1c2d84b2ebc5797e3a73f04be反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in CH2Cl2 (50 ml) was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, dried the clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a H2O bath at 60° C. without vacuum Once most solvent had been evaporated off dried the clear oil under high vacuum at RT for 30 min.
来源 ID: ord-024d92b394694f529710f777db8a6fd5反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in 50 ml of CH2Cl2 was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, it was furthered dried to a clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a H2O bath at 60° C. without vacuum Once most solvent had been evaporated off it was furthered dried to a clear oil under high vacuum at RT for 30 min.
来源 ID: ord-11ed25a29ee7437a8423d0f7ff9e26f8反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in 50 ml of CH2Cl2 was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, it was furthered dried to a clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a H2O bath at 60° C. without vacuum Once most solvent had been evaporated off it was furthered dried to a clear oil under high vacuum at RT for 30 min.
来源 ID: ord-11ed25a29ee7437a8423d0f7ff9e26f8反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in 50 ml of CH2Cl2 was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, it was furthered dried to a clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a H2O bath at 60° C. without vacuum Once most solvent had been evaporated off it was furthered dried to a clear oil under high vacuum at RT for 30 min.
来源 ID: ord-454d7df1c2d84b2ebc5797e3a73f04be反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-df10238793684e25a82a19da1f7d9d09反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in 50 ml of CH2Cl2 was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, it was furthered dried to a clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a H2O bath at 60° C. without vacuum Once most solvent had been evaporated off it was furthered dried to a clear oil under high vacuum at RT for 30 min.
来源 ID: ord-eaa68f1bcc884a5b95a4f6b73979baf2反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in 50 ml of CH2Cl2 was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, it was furthered dried to a clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a H2O bath at 60° C. without vacuum Once most solvent had been evaporated off it was furthered dried to a clear oil under high vacuum at RT for 30 min.
来源 ID: ord-eaa68f1bcc884a5b95a4f6b73979baf2反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in CH2Cl2 (50 ml) was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a water bath at 60° C. without vacuum. Once most solvent had been evaporated off, dried the clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a water bath at 60° C. without vacuum Once most solvent had been evaporated off dried the clear oil under high vacuum at RT for 30 min.
来源 ID: ord-9562010fe65444b0bea2481bd49ac41a反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in CH2Cl2 (50 ml) was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a water bath at 60° C. without vacuum. Once most solvent had been evaporated off, dried the clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a water bath at 60° C. without vacuum Once most solvent had been evaporated off dried the clear oil under high vacuum at RT for 30 min.
来源 ID: ord-9562010fe65444b0bea2481bd49ac41a反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in CH2Cl2 (50 ml) was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2 N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a water bath at 60° C. without vacuum. Once most solvent had been evaporated off, dried the clear oil under high vacuum at RT for 30 min. The reaction flask was vented during the exothermic addition After the addition washed first with about 60 ml 2N HCl with about 60 ml of a mix of 2 N NaOH and brine The organic layer was dried over Na2SO4 The solution was evaporated by heating in a water bath at 60° C. without vacuum Once most solvent had been evaporated off dried the clear oil under high vacuum at RT for 30 min.
来源 ID: ord-7c5b175751264ef5956c6d365f04fd1dPubChem References
以下资料来自该化合物的公开数据库参考记录。
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