反应 #4054144
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-e9a1b3b2ee4a4d2a9a387d79154091ea暂无可渲染的结构数据
CN(C)CCCOC1=CC=C(C=C1)CN中间体产品
3-[4-(aminomethyl)phenoxy]-N,N-dimethylpropan-1-amine
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | 4 - [3 - (二甲氨基)丙氧基]苄胺 |
|---|---|
| English name | 3-[4-(aminomethyl)phenoxy]-N,N-dimethylpropan-1-amine |
| IUPAC 名称 | — |
| CAS号 | 91637-76-2 |
| 数据库编号 | 21465384 |
| 分子式 | — |
| 分子量 | — |
产品信息
4 - [3 - (二甲氨基)丙氧基]苄胺(CAS 91637-76-2)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 21465384
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e9a1b3b2ee4a4d2a9a387d79154091ea反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-b8d6d6004db044edbc0ea654bcd59dd4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-f19a3ac27579445594d6d818817dc83d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-f19a3ac27579445594d6d818817dc83d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-3e6a40bfeb16469da8fd64d469e0f5d1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-3e6a40bfeb16469da8fd64d469e0f5d1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e9a1b3b2ee4a4d2a9a387d79154091ea反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-0d3d4d386feb4faabda01e1db0770d9c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-b7b04f4deecc4e139729fe242186fe1b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-b8d6d6004db044edbc0ea654bcd59dd4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-f19a3ac27579445594d6d818817dc83d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-(3-(Dimethylamino)propoxy)benzonitrile (300 mg) in methanol (20 mL) was treated with Raney nickel (wet, 1.5 g) under H2 (30 psi) for 4 hour. The insoluble material was filtered off and the filtrate was concentrated to provide the title compound. The insoluble material was filtered off the filtrate was concentrated
来源 ID: ord-3e6a40bfeb16469da8fd64d469e0f5d1PubChem 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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