反应 #4177002
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-6a6f7e1b9b004cf195e59e8a16ce4226暂无可渲染的结构数据
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4-氨基丁酸乙酯(CAS 5959-36-4)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。
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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-6a6f7e1b9b004cf195e59e8a16ce4226反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-823a2b254031493d8cdef0b384e2cfef反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b74607ab02e547a1bf301e90ea0093eb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-88a0c1cac4d54b75824e52fee8e6a3c0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1e45b74e91a2417aa2619c63f58d04eb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-823a2b254031493d8cdef0b384e2cfef反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b74607ab02e547a1bf301e90ea0093eb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b74607ab02e547a1bf301e90ea0093eb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-88a0c1cac4d54b75824e52fee8e6a3c0反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1e45b74e91a2417aa2619c63f58d04eb反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of powdered potassium carbonate (14.0 g, 96.2 mmol, 5 equiv.), ethyl-4-aminobutyrate (IVb) (6.5 g, 38.6 mmol, 2 equiv.) and methanesulfonic acid (R)-1-carbamoyl-propyl ester (IIi) (3.5 g, 19.3 mmol, 1 equiv.) in acetonitrile (40 ml, 11 vol.) is heated to 80° C. for 17 hours. The mixture is then filtered and the cake rinsed with acetonitrile (30 ml). Combined filtrates are concentrated to dryness under reduced pressure. The crude methyl-(S)-4-(1-carbamoylpropylamino)butyrate (VIg) obtained as a yellow oil is used directly in the next step. The mixture is then filtered the cake rinsed with acetonitrile (30 ml) Combined filtrates are concentrated to dryness under reduced pressure
来源 ID: ord-72c363b4584a4c4282ee76fa16dcfa0e反应条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of powdered caesium carbonate (9.0 g, 27.4 mmol, 5 equiv.), ethyl-4-aminobutyrate (IVb) (1.85 g, 11.0 mmol, 2 equiv.) and methanesulfonic acid (R)-1-carbamoyl-propyl ester (IIi) (1.0 g, 5.5 mmol, 1 equiv.) in acetonitrile (20 ml, 20 vol.) is heated to 60° C. for 16 hours. The mixture is then filtered and the cake rinsed with acetonitrile (50 ml). Combined filtrates are concentrated to dryness under reducd pressure. The crude methyl-(R)-4-(1-carbamoylpropylamino)butyrate is used directly in the next step. The mixture is then filtered the cake rinsed with acetonitrile (50 ml) Combined filtrates are concentrated to dryness under reducd pressure
来源 ID: ord-d6dace805175480cba2f21e509d3e6baPubChem References
以下资料来自该化合物的公开数据库参考记录。
