反应 #4154446
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-754452251f8046a59b1a712c361b3af2暂无可渲染的结构数据
COC(=O)C1CCCCN1产品信息
2-哌啶甲酸甲酯(CAS 41994-45-0)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-754452251f8046a59b1a712c361b3af2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-54fe4ead200749f5bb709f3347b08feb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e159ed65168a47ce8c018446435d0cde反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c829f1bee7ff48aba1e02480f88e5388反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1ec546d0ebf34c00beb5ace81eaa34de反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-11d0c2f349e64b3492cfa9bbd6169df7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-12f228414a114b2d91d07c477b718813反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-754452251f8046a59b1a712c361b3af2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-54fe4ead200749f5bb709f3347b08feb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Piperidenemethanol was made from methyl pipecolinate as described in Method B1b. The 2-hydroxyethylamine was converted to 2-chloromethylpiperidinium chloride according to Method B7a. 2-Methyl4-nitrophenyl isothiocyanate was reacted with 2-chloromethylpiperidinium chloride according according to Method C1a to give 9-(2-methyl-4-nitrophenylimino)-1-aza-8-thiabicyclo[4.3.0]nonane.
来源 ID: ord-c951ff5debe4466ebad410dd29a6a027反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 2-Piperidenemethanol was made from methyl pipecolinate as described in Method B1b. The 2-hydroxyethylamine was converted to 2-chloromethylpiperidinium chloride according to Method B7a. 2-Methyl4-nitrophenyl isothiocyanate was reacted with 2-chloromethylpiperidinium chloride according according to Method C1a to give 9-(2-methyl-4-nitrophenylimino)-1-aza-8-thiabicyclo[4.3.0]nonane.
来源 ID: ord-c951ff5debe4466ebad410dd29a6a027反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Methyl 6-chloro-5-nitronicotinate (2.0 g, 9.23 mmol) was added to methyl piperidine-2-carboxylate (5.2 g, 36.92 mmol) while stirring at room temperature. The viscous yellow reaction was heated to 90° C. for one h and then allowed to cool back to room temperature. The reaction was diluted with dichloromethane (20 mL) and purified via column chromatography (220 g SiO2, 20-30% gradient, ethyl acetate in hexanes) to yield the title compound (2.95 g, 99% yield) as a yellow oil. [M+H] calc'd for C14H17N3O6, 324. found, 324. The viscous yellow reaction was heated to 90° C. for one h to cool back to room temperature purified via column chromatography (220 g SiO2, 20-30% gradient, ethyl acetate in hexanes)
来源 ID: ord-68cbb686c28540b9aac9f1ba27ee8fe5PubChem References
以下资料来自该化合物的公开数据库参考记录。
