反应 #3849048
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-df322c2a1eb5430b8191fef5c36c5a47暂无可渲染的结构数据
CC1=C(C(=CC=C1)C=O)N(C)C产品信息
2-(二甲氨基)-3-甲基苯甲醛(CAS 87067-13-8)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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合成路线数据
5 条反应 · 5 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-df322c2a1eb5430b8191fef5c36c5a47反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of Compound 150 (0.17 g, 0.81 mmol) in Et2O (5.0 mL) at −78° C. under Argon atmosphere was added dropwise a solution of 1.7M t-BuLi in pentane (1.0 mL, 1.79 mmol), and the reaction was stirred for 1 h. DMF (0.25 mL, 3.24 mmol) was added, and the cooling bath was removed. After 1h15, the reaction was cooled to 0° C., and saturated NH4Cl was added. The mixture was extracted with EtOAc, washed with brine, dried over MgSO4, and filtered. The solvent was removed, and the residue was purified by silica gel flash chromatography with EtOAc (15%) and hexanes (85%) as eluent to produce Compound 151 as a yellow oil. the cooling bath was removed saturated NH4Cl was added The mixture was extracted with EtOAc washed with brine dried over MgSO4 filtered The solvent was removed the residue was purified by silica gel flash chromatography with EtOAc (15%) and hexanes (85%) as eluent
来源 ID: ord-e9def0dcc01c49aeb9e729b45933fda2反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of Compound 150 (0.17 g, 0.81 mmol) in Et2O (5.0 mL) at −78° C. under Argon atmosphere was added dropwise a solution of 1.7M t-BuLi in pentane (1.0 mL, 1.79 mmol), and the reaction was stirred for 1 h. DMF (0.25 mL, 3.24 mmol) was added, and the cooling bath was removed. After 1h15, the reaction was cooled to 0° C., and saturated NH4Cl was added. The mixture was extracted with EtOAc, washed with brine, dried over MgSO4, and filtered. The solvent was removed, and the residue was purified by silica gel flash chromatography with EtOAc (15%) and hexanes (85%) as eluent to produce Compound 151 as a yellow oil. the cooling bath was removed saturated NH4Cl was added The mixture was extracted with EtOAc washed with brine dried over MgSO4 filtered The solvent was removed the residue was purified by silica gel flash chromatography with EtOAc (15%) and hexanes (85%) as eluent
来源 ID: ord-e9def0dcc01c49aeb9e729b45933fda2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-df322c2a1eb5430b8191fef5c36c5a47反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of Compound 150 (0.17 g, 0.81 mmol) in Et2O (5.0 mL) at −78° C. under Argon atmosphere was added dropwise a solution of 1.7M t-BuLi in pentane (1.0 mL, 1.79 mmol), and the reaction was stirred for 1 h. DMF (0.25 mL, 3.24 mmol) was added, and the cooling bath was removed. After 1h15, the reaction was cooled to 0° C., and saturated NH4Cl was added. The mixture was extracted with EtOAc, washed with brine, dried over MgSO4, and filtered. The solvent was removed, and the residue was purified by silica gel flash chromatography with EtOAc (15%) and hexanes (85%) as eluent to produce Compound 151 as a yellow oil. the cooling bath was removed saturated NH4Cl was added The mixture was extracted with EtOAc washed with brine dried over MgSO4 filtered The solvent was removed the residue was purified by silica gel flash chromatography with EtOAc (15%) and hexanes (85%) as eluent
来源 ID: ord-e9def0dcc01c49aeb9e729b45933fda2PubChem References
以下资料来自该化合物的公开数据库参考记录。
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