反应 #4085193
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-546a3edae89a43af9fe4d5b4bea03bfc暂无可渲染的结构数据
C1CCNC(C1)C(=O)OCC2=CC=CC=C2产品信息
苄基哌啶-2-羧酸酯(CAS 38068-75-6)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-546a3edae89a43af9fe4d5b4bea03bfc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d45cd598ce2f468ba03ab28e398df9b4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a09cfde997aa425d8d18540bd4414466反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-79c2595df6e54b8c974d46ad651c5bcd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Benzyl pipecolate was routinely generated by treating an ethyl acetate suspension of this salt with saturated sodium bicarbonate until dissolution of the organic material. The aqueous layer was extracted twice with ethyl acetate and the combined organic extracts were dried with MgSO4 and evaporated to yield (S)-Benzyl pipecolate (133) as a pale yellow oil. by treating until dissolution of the organic material The aqueous layer was extracted twice with ethyl acetate the combined organic extracts were dried with MgSO4 evaporated
来源 ID: ord-a1a196c1d37c4c3f9bf2e3b0eeb99535反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Benzyl pipecolate was routinely generated by treating an ethyl acetate suspension of this salt with saturated sodium bicarbonate until dissolution of the organic material. The aqueous layer was extracted twice with ethyl acetate and the combined organic extracts were dried with MgSO4 and evaporated to yield (S)-Benzyl pipecolate (133) as a pale yellow oil. by treating until dissolution of the organic material The aqueous layer was extracted twice with ethyl acetate the combined organic extracts were dried with MgSO4 evaporated
来源 ID: ord-a1a196c1d37c4c3f9bf2e3b0eeb99535反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Benzyl pipecolate was routinely generated by treating an ethyl acetate suspension of this salt with saturated sodium bicarbonate until dissolution of the organic material. The aqueous layer was extracted twice with ethyl acetate and the combined organic extracts were dried with MgSO4 and evaporated to yield (S)-Benzyl pipecolate (15) as a pale yellow oil. by treating until dissolution of the organic material The aqueous layer was extracted twice with ethyl acetate the combined organic extracts were dried with MgSO4 evaporated
来源 ID: ord-f218f10babd54387b3ff407e2cd3e023反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-546a3edae89a43af9fe4d5b4bea03bfc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d45cd598ce2f468ba03ab28e398df9b4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Benzyl pipecolate was routinely generated by treating an ethyl acetate suspension of this salt with saturated sodium bicarbonate until dissolution of the organic material. The aqueous layer was extracted twice with ethyl acetate and the combined organic extracts were dried with MgSO4 and evaporated to yield (S)-Benzyl pipecolate (15) as a pale yellow oil. by treating until dissolution of the organic material The aqueous layer was extracted twice with ethyl acetate the combined organic extracts were dried with MgSO4 evaporated
来源 ID: ord-f218f10babd54387b3ff407e2cd3e023反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-79c2595df6e54b8c974d46ad651c5bcd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Benzyl pipecolate was routinely generated by treating an ethyl acetate suspension of this salt with saturated sodium bicarbonate until dissolution of the organic material. The aqueous layer was extracted twicewith ethyl acetate and the combined organic extracts were dried with MgSO4 and evaporated to yield (S)-Benzyl pipecolate (133) as a pale yellow oil. by treating until dissolution of the organic material The aqueous layer was extracted twicewith ethyl acetate the combined organic extracts were dried with MgSO4 evaporated
来源 ID: ord-97f290ebe37e413da4a3a0b19c1bd375PubChem References
以下资料来自该化合物的公开数据库参考记录。
