反应 #4120660
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-1db7147b95684f38b3bdf16a977d8ee7暂无可渲染的结构数据
CC(C)N(CC1=CC=C(C=C1)Br)C(C)C中间体产品
N-[(4-bromophenyl)methyl]-N-propan-2-ylpropan-2-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 | N-(4-溴苯甲基)-N-异丙基丙烷-2-胺 |
|---|---|
| English name | N-[(4-bromophenyl)methyl]-N-propan-2-ylpropan-2-amine |
| IUPAC 名称 | — |
| CAS号 | 98816-61-6 |
| 数据库编号 | 598770 |
| 分子式 | — |
| 分子量 | — |
产品信息
N-(4-溴苯甲基)-N-异丙基丙烷-2-胺(CAS 98816-61-6)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 598770
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
10 条反应 · 10 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1db7147b95684f38b3bdf16a977d8ee7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N-(4-bromobenzyl)-N,N-diisopropylamine (2.3 g) in THF (10 ml) was added dropwise at −78° C. n-BuLi (1.6 mmol/ml hexane solution, 3.8 ml). Ten minutes later, N,O-dimethyl-N-(1-trityl-piperidine-4-carbonyl)hydroxylamine (1.5 g) in THF (20 ml) was added dropwise to the mixture, and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added ammonium chloride aqueous solution, and the mixture was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ethyl acetate The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-4e0682a8042f420a89b225e795ace753反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N-(4-bromobenzyl)-N,N-diisopropylamine (2.3 g) in THF (10 ml) was added dropwise at −78° C. n-BuLi (1.6 mmol/ml hexane solution, 3.8 ml). Ten minutes later, N,O-dimethyl-N-(1-trityl-piperidine-4-carbonyl)hydroxylamine (1.5 g) in THF (20 ml) was added dropwise to the mixture, and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added ammonium chloride aqueous solution, and the mixture was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ethyl acetate The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-4e0682a8042f420a89b225e795ace753反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-bromobenzylbromide (5.0 g), N,N-diisopropylamine (7.85 ml) and potassium carbonate (2.76 g) in dimethylformamide (50 ml) was stirred at 80° C. for 2 hours. To the mixture was added water, and the mixture was extracted with ether. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ether The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-0947629a38f245a280dfe00ef647a3cd反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-bromobenzylbromide (5.0 g), N,N-diisopropylamine (7.85 ml) and potassium carbonate (2.76 g) in dimethylformamide (50 ml) was stirred at 80° C. for 2 hours. To the mixture was added water, and the mixture was extracted with ether. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ether The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-0947629a38f245a280dfe00ef647a3cd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N-(4-bromobenzyl)-N,N-diisopropylamine (2.3 g) in THF (10 ml) was added dropwise at −78° C. n-BuLi (1.6 mmol/ml hexane solution, 3.8 ml). Ten minutes later, N,O-dimethyl-N-(1-trityl-piperidine-4-carbonyl)hydroxylamine (1.5 g) in THF (20 ml) was added dropwise to the mixture, and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added ammonium chloride aqueous solution, and the mixture was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ethyl acetate The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-4e0682a8042f420a89b225e795ace753反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-bromobenzylbromide (5.0 g), N,N-diisopropylamine (7.85 ml) and potassium carbonate (2.76 g) in dimethylformamide (50 ml) was stirred at 80° C. for 2 hours. To the mixture was added water, and the mixture was extracted with ether. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ether The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-0947629a38f245a280dfe00ef647a3cd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1db7147b95684f38b3bdf16a977d8ee7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of N-(4-bromobenzyl)-N,N-diisopropylamine (2.3 g) in THF (10 ml) was added dropwise at −78° C. n-BuLi (1.6 mmol/ml hexane solution, 3.8 ml). Ten minutes later, N,O-dimethyl-N-(1-trityl-piperidine-4-carbonyl)hydroxylamine (1.5 g) in THF (20 ml) was added dropwise to the mixture, and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added ammonium chloride aqueous solution, and the mixture was extracted with ethyl acetate. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ethyl acetate The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-4e0682a8042f420a89b225e795ace753反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-bromobenzylbromide (5.0 g), N,N-diisopropylamine (7.85 ml) and potassium carbonate (2.76 g) in dimethylformamide (50 ml) was stirred at 80° C. for 2 hours. To the mixture was added water, and the mixture was extracted with ether. The extract was washed with water, dried (MgSO4) and concentrated to give the title compound (5.0 g). the mixture was extracted with ether The extract was washed with water dried (MgSO4) concentrated
来源 ID: ord-0947629a38f245a280dfe00ef647a3cdPubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 1039970-32-5
CAS 1503055-02-4
CAS 1353965-03-3
CAS 1513614-25-9
CAS 1856112-50-9
CAS 1784522-94-6
CAS 1050214-15-7
CAS 1609402-88-1
CAS 1096314-34-9
CAS 1044924-69-7
CAS 1704082-56-3
CAS 60376-97-8
