反应 #4099240
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-a597d3907a89441badf38fa79286c204暂无可渲染的结构数据
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N-(2-苯基乙基)丁-3-烯-1-胺(CAS 867324-06-9)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-a597d3907a89441badf38fa79286c204反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 1 (12.6 g, 49.75 mmol) in THF (200 mL) is added KOTMS (6.38 g, 49.75 mmol). The mixture is stirred overnight at room temperature. The mixture is concentrated and the residue dissolved in dichloromethane (200 mL) and cooled to 0° C. Trimethylacetyl chloride (5.94 g, 49.25 mmol) is added slowly and the mixture is warmed to room temperature over 2 hours. The mixture is cooled to −78° C., 2 (8.63 g, 49.25 mmol) is added and stirring continued at −78° C. for 1.5 h. Saturated sodium bicarbonate (100 mL) is added and the mixture is allowed to warm to rt. The mixture is extracted with EtOAc (4×100 mL) and the organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 15 g (76%) of the title compound as a mixture of two diastereomers in an equimolecular ratio. M+H+=399.37. The mixture is concentrated the residue dissolved in dichloromethane (200 mL) cooled to 0° C the mixture is warmed to room temperature over 2 hours The mixture is cooled to −78° C. stirring continued at −78° C. for 1.5 h to warm to rt The mixture is extracted with EtOAc (4×100 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-69cf5403e4eb400ca81dd051f336b710反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-phenylethylamine (72 mL, 570 mmol) is added K2CO3 (82 g, 570 mmol) and 4-bromo-1-butene (25 g, 185 mmol). The solution is stirred overnight at room temperature. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added. The mixture is extracted with EtOAc (4×150 mL). The organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 20 g (62%) of the title compound. M+H+=176.10. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added The mixture is extracted with EtOAc (4×150 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-4a6da6a3988b47f2a7ec0756122c8c30反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 1 (12.6 g, 49.75 mmol) in THF (200 mL) is added KOTMS (6.38 g, 49.75 mmol). The mixture is stirred overnight at room temperature. The mixture is concentrated and the residue dissolved in dichloromethane (200 mL) and cooled to 0° C. Trimethylacetyl chloride (5.94 g, 49.25 mmol) is added slowly and the mixture is warmed to room temperature over 2 hours. The mixture is cooled to −78° C., 2 (8.63 g, 49.25 mmol) is added and stirring continued at −78° C. for 1.5 h. Saturated sodium bicarbonate (100 mL) is added and the mixture is allowed to warm to rt. The mixture is extracted with EtOAc (4×100 mL) and the organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 15 g (76%) of the title compound as a mixture of two diastereomers in an equimolecular ratio. M+H+=399.37. The mixture is concentrated the residue dissolved in dichloromethane (200 mL) cooled to 0° C the mixture is warmed to room temperature over 2 hours The mixture is cooled to −78° C. stirring continued at −78° C. for 1.5 h to warm to rt The mixture is extracted with EtOAc (4×100 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-4b4676d8f0c54914b0b770a60ef616ca反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-phenylethylamine (72 mL, 570 mmol) is added K2CO3 (82 g, 570 mmol) and 4-bromo-1-butene (25 g, 185 mmol). The solution is stirred overnight at room temperature. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added. The mixture is extracted with EtOAc (4×150 mL). The organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 20 g (62%) of the title compound. M+H+=176.10. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added The mixture is extracted with EtOAc (4×150 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-65898676a2d449a5a2b0568fca6d3bd3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 1 (12.6 g, 49.75 mmol) in THF (200 mL) is added KOTMS (6.38 g, 49.75 mmol). The mixture is stirred overnight at room temperature. The mixture is concentrated and the residue dissolved in dichloromethane (200 mL) and cooled to 0° C. Trimethylacetyl chloride (5.94 g, 49.25 mmol) is added slowly and the mixture is warmed to room temperature over 2 hours. The mixture is cooled to −78° C., 2 (8.63 g, 49.25 mmol) is added and stirring continued at −78° C. for 1.5 h. Saturated sodium bicarbonate (100 mL) is added and the mixture is allowed to warm to rt. The mixture is extracted with EtOAc (4×100 mL) and the organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 15 g (76%) of the title compound as a mixture of two diastereomers in an equimolecular ratio. M+H+=399.37. The mixture is concentrated the residue dissolved in dichloromethane (200 mL) cooled to 0° C the mixture is warmed to room temperature over 2 hours The mixture is cooled to −78° C. stirring continued at −78° C. for 1.5 h to warm to rt The mixture is extracted with EtOAc (4×100 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-69cf5403e4eb400ca81dd051f336b710反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-phenylethylamine (72 mL, 570 mmol) is added K2CO3 (82 g, 570 mmol) and 4-bromo-1-butene (25 g, 185 mmol). The solution is stirred overnight at room temperature. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added. The mixture is extracted with EtOAc (4×150 mL). The organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 20 g (62%) of the title compound. M+H+=176.10. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added The mixture is extracted with EtOAc (4×150 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-4a6da6a3988b47f2a7ec0756122c8c30反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a597d3907a89441badf38fa79286c204反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 1 (12.6 g, 49.75 mmol) in THF (200 mL) is added KOTMS (6.38 g, 49.75 mmol). The mixture is stirred overnight at room temperature. The mixture is concentrated and the residue dissolved in dichloromethane (200 mL) and cooled to 0° C. Trimethylacetyl chloride (5.94 g, 49.25 mmol) is added slowly and the mixture is warmed to room temperature over 2 hours. The mixture is cooled to −78° C., 2 (8.63 g, 49.25 mmol) is added and stirring continued at −78° C. for 1.5 h. Saturated sodium bicarbonate (100 mL) is added and the mixture is allowed to warm to rt. The mixture is extracted with EtOAc (4×100 mL) and the organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 15 g (76%) of the title compound as a mixture of two diastereomers in an equimolecular ratio. M+H+=399.37. The mixture is concentrated the residue dissolved in dichloromethane (200 mL) cooled to 0° C the mixture is warmed to room temperature over 2 hours The mixture is cooled to −78° C. stirring continued at −78° C. for 1.5 h to warm to rt The mixture is extracted with EtOAc (4×100 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-4b4676d8f0c54914b0b770a60ef616ca反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-phenylethylamine (72 mL, 570 mmol) is added K2CO3 (82 g, 570 mmol) and 4-bromo-1-butene (25 g, 185 mmol). The solution is stirred overnight at room temperature. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added. The mixture is extracted with EtOAc (4×150 mL). The organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 20 g (62%) of the title compound. M+H+=176.10. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added The mixture is extracted with EtOAc (4×150 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-65898676a2d449a5a2b0568fca6d3bd3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 1 (12.6 g, 49.75 mmol) in THF (200 mL) is added KOTMS (6.38 g, 49.75 mmol). The mixture is stirred overnight at room temperature. The mixture is concentrated and the residue dissolved in dichloromethane (200 mL) and cooled to 0° C. Trimethylacetyl chloride (5.94 g, 49.25 mmol) is added slowly and the mixture is warmed to room temperature over 2 hours. The mixture is cooled to −78° C., 2 (8.63 g, 49.25 mmol) is added and stirring continued at −78° C. for 1.5 h. Saturated sodium bicarbonate (100 mL) is added and the mixture is allowed to warm to rt. The mixture is extracted with EtOAc (4×100 mL) and the organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 15 g (76%) of the title compound as a mixture of two diastereomers in an equimolecular ratio. M+H+=399.37. The mixture is concentrated the residue dissolved in dichloromethane (200 mL) cooled to 0° C the mixture is warmed to room temperature over 2 hours The mixture is cooled to −78° C. stirring continued at −78° C. for 1.5 h to warm to rt The mixture is extracted with EtOAc (4×100 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-7169ec6c35c343c491b32a76fe3a9421反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 2-phenylethylamine (72 mL, 570 mmol) is added K2CO3 (82 g, 570 mmol) and 4-bromo-1-butene (25 g, 185 mmol). The solution is stirred overnight at room temperature. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added. The mixture is extracted with EtOAc (4×150 mL). The organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 20 g (62%) of the title compound. M+H+=176.10. The solution is evaporated to dryness and H2O/EtOAc (1:1) (600 mL) is added The mixture is extracted with EtOAc (4×150 mL) dried concentrated under vacuum The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)
来源 ID: ord-819fabff854e4a8caef24ba9fe01ed0ePubChem References
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