反应 #4140026
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-65d28985425b49dbaebc49e6762771f6暂无可渲染的结构数据
CCOC(=O)C(C)CCBr产品信息
乙基 4-溴-2-甲基丁酸酯(CAS 2213-09-4)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-65d28985425b49dbaebc49e6762771f6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a54f72d3f7a34f16a27307415a58d20a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ce82d1b5c0614cf7965e13dea5cc3472反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-65d28985425b49dbaebc49e6762771f6反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-65d28985425b49dbaebc49e6762771f6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 40.0 g. (0.19 mole) of ethyl 4-bromo-2-methylbutyrate (Tetrahedron 21, 2966 (1965)), 66.0 g. (0.76 mole) of morpholine and 750 ml. of benzene was heated at 60°C. for 5 hours and stirred at room temperature for a total of 40 hours. A colorless solid was removed by filtration, and the mother liquor was evaporated to give a colorless, mobile residue. This material was combined with 250 ml. of ether and filtered to remove a small amount of additional solid. The solution was concentrated and the residue distilled to give the desired material as 38.0 g. (93%) of colorless liquid (b.p. 71°-73°C. at 0.10 mm). A mixture of 40.0 g A colorless solid was removed by filtration the mother liquor was evaporated to give a colorless, mobile residue of ether and filtered to remove a small amount of additional solid The solution was concentrated the residue distilled
来源 ID: ord-3b6645cb1cf4455798acf0fc34c234e3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 40.0 g. (0.19 mole) of ethyl 4-bromo-2-methylbutyrate (Tetrahedron 21, 2966 (1965)), 66.0 g. (0.76 mole) of morpholine and 750 ml. of benzene was heated at 60°C. for 5 hours and stirred at room temperature for a total of 40 hours. A colorless solid was removed by filtration, and the mother liquor was evaporated to give a colorless, mobile residue. This material was combined with 250 ml. of ether and filtered to remove a small amount of additional solid. The solution was concentrated and the residue distilled to give the desired material as 38.0 g. (93%) of colorless liquid (b.p. 71°-73°C. at 0.10 mm). A mixture of 40.0 g A colorless solid was removed by filtration the mother liquor was evaporated to give a colorless, mobile residue of ether and filtered to remove a small amount of additional solid The solution was concentrated the residue distilled
来源 ID: ord-3b6645cb1cf4455798acf0fc34c234e3反应条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 10.5 g. (0.05 mole) of ethyl γ-bromo-α-methylbutyrate was combined with 17.0 g. (0.20 mole) of piperidine and 100 ml. of benzene and stirred for 16 hours at room temperature and heated at 60° C. for 4 hours. The reaction mixture was cooled and the colorless solid which appeared was removed by filtration. The mother liquor was concentrated to give ethyl α-methyl-γ-piperidinobutyrate as a mobile yellow liquid which distilled (b.p. 78° C. at 0.25 mm.) as 6.7 g. (63%) of colorless liquid. The nuclear magnetic resonance and infrared spectra were consistent with the desired compound. The reaction mixture was cooled the colorless solid which appeared was removed by filtration The mother liquor was concentrated
来源 ID: ord-5285d10f4538403f9ea38ebefec88d98反应条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 10.5 g. (0.05 mole) of ethyl γ-bromo-α-methylbutyrate was combined with 17.0 g. (0.20 mole) of piperidine and 100 ml. of benzene and stirred for 16 hours at room temperature and heated at 60° C. for 4 hours. The reaction mixture was cooled and the colorless solid which appeared was removed by filtration. The mother liquor was concentrated to give ethyl α-methyl-γ-piperidinobutyrate as a mobile yellow liquid which distilled (b.p. 78° C. at 0.25 mm.) as 6.7 g. (63%) of colorless liquid. The nuclear magnetic resonance and infrared spectra were consistent with the desired compound. The reaction mixture was cooled the colorless solid which appeared was removed by filtration The mother liquor was concentrated
来源 ID: ord-5285d10f4538403f9ea38ebefec88d98反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 40.0 g. (0.19 mole) of ethyl 4-bromo-2-methylbutyrate (Tetrahedron 21, 2966 (1965)), 66.0 g. (0.76 mole) of morpholine and 750 ml. of benzene was heated at 60°C. for 5 hours and stirred at room temperature for a total of 40 hours. A colorless solid was removed by filtration, and the mother liquor was evaporated to give a colorless, mobile residue. This material was combined with 250 ml. of ether and filtered to remove a small amount of additional solid. The solution was concentrated and the residue distilled to give the desired material as 38.0 g. (93%) of colorless liquid (b.p. 71°-73°C. at 0.10 mm). A mixture of 40.0 g A colorless solid was removed by filtration the mother liquor was evaporated to give a colorless, mobile residue of ether and filtered to remove a small amount of additional solid The solution was concentrated the residue distilled
来源 ID: ord-3b6645cb1cf4455798acf0fc34c234e3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a54f72d3f7a34f16a27307415a58d20a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ce82d1b5c0614cf7965e13dea5cc3472PubChem References
以下资料来自该化合物的公开数据库参考记录。
