反应 #4140864
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-942247e783c74c34bfad1ff0571da6c3暂无可渲染的结构数据
CCOC(=O)C(C)(C)CBr产品信息
乙基 3-溴-2,2-二甲基丙酸酯(CAS 2843-18-7)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-942247e783c74c34bfad1ff0571da6c3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1a3ec449d99544a1b2389d2d0ef2d366反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e6756b197def4b5e83c2d4e785df2ea3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f75a066b0b1d4b6d9ed6d273f63db96c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-Bromo-2,2-dimethylpropanoic acid (200 mg) was dissolved in EtOH (5 ml) and treated with concentrated H2SO4 (0.4 ml). This mixture was heated at reflux overnight then evaporated. The residue was extracted from H2O with EtOAc (×2) and the combined organic solutions dried and evaporated to give the title compound (316 mg) as a clear oil. δH (CDCl3, 400 MHz) 1.20 (3H, t), 1.32 (6H, s), 3.51 (2H, s), 4.18 (2H, q). This mixture was heated at reflux overnight then evaporated The residue was extracted from H2O with EtOAc (×2) the combined organic solutions dried evaporated
来源 ID: ord-a01ad34764be4e8ca509ba0e5feb857c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-942247e783c74c34bfad1ff0571da6c3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-942247e783c74c34bfad1ff0571da6c3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-Bromo-2,2-dimethylpropanoic acid (200 mg) was dissolved in EtOH (5 ml) and treated with concentrated H2SO4 (0.4 ml). This mixture was heated at reflux overnight then evaporated. The residue was extracted from H2O with EtOAc (×2) and the combined organic solutions dried and evaporated to give the title compound (316 mg) as a clear oil. δH (CDCl3, 400 MHz) 1.20 (3H, t), 1.32 (6H, s), 3.51 (2H, s), 4.18 (2H, q). This mixture was heated at reflux overnight then evaporated The residue was extracted from H2O with EtOAc (×2) the combined organic solutions dried evaporated
来源 ID: ord-a01ad34764be4e8ca509ba0e5feb857c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-Bromo-2,2-dimethylpropanoic acid (200 mg) was dissolved in EtOH (5 ml) and treated with concentrated H2SO4 (0.4 ml). This mixture was heated at reflux overnight then evaporated. The residue was extracted from H2O with EtOAc (×2) and the combined organic solutions dried and evaporated to give the title compound (316 mg) as a clear oil. δH (CDCl3, 400 MHz) 1.20 (3H, t), 1.32 (6H, s), 3.51 (2H, s), 4.18 (2H, q). This mixture was heated at reflux overnight then evaporated The residue was extracted from H2O with EtOAc (×2) the combined organic solutions dried evaporated
来源 ID: ord-a01ad34764be4e8ca509ba0e5feb857c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1a3ec449d99544a1b2389d2d0ef2d366反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e6756b197def4b5e83c2d4e785df2ea3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f75a066b0b1d4b6d9ed6d273f63db96cPubChem References
以下资料来自该化合物的公开数据库参考记录。
