反应 #4026847
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-d03357266a1f4b39971c556edc2dc47f暂无可渲染的结构数据
C1CN(CCC1NC(=O)C2=CC=CC=C2)CC3=CC=CC=C3产品信息
N-苄基-4-苯甲酰氨基哌啶(CAS 971-34-6)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。
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8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d03357266a1f4b39971c556edc2dc47f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 10% palladium on carbon (0.2 g) in 30 mL of ethyl alcohol was added a solution of 1-benzyl-4-benzamido-piperidine (0.5 g, 1.79 mmol) in ethyl alcohol (10 mL). The resulting suspension was hydrogenated at 100 psi at 50° C. for 30 h after which it was filtered through a pad of celite and the solvent was removed in vacuo to obtain 0.34 g (100%) of 4-benzamidopiperidine as a white solid. It was used in the next step without purification. after which it was filtered through a pad of celite the solvent was removed in vacuo
来源 ID: ord-2f29796371034863a69c1bad23542458反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 10% palladium on carbon (0.2 g) in 30 mL of ethyl alcohol was added a solution of 1-benzyl-4-benzamido-piperidine (0.5 g, 1.79 mmol) in ethyl alcohol (10 mL). The resulting suspension was hydrogenated at 100 psi at 50° C. for 30 h after which it was filtered through a pad of celite and the solvent was removed in vacuo to obtain 0.34 g (100%) of 4-benzamidopiperidine as a white solid. It was used in the next step without purification. after which it was filtered through a pad of celite the solvent was removed in vacuo
来源 ID: ord-2f29796371034863a69c1bad23542458反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a biphasic solution of 4-amino-1-benzylpiperidine (6.0 g, 31.6 mmol), K2CO3 (8.71 g, 63.1 mmol) in CH2Cl2 (200 mL) and water (100 mL) was added benzoyl chloride (4.86 g, 34.7 mmol) in 20 mL of CH2Cl2 at 0° C. with stirring. After stirring for 4 h at room temperature, the layers were separated. The organic layer was washed with water, dried over MgSO4 and filtered. The solvent was removed in vacuo to obtain 1-benzyl-4-benzamidopiperidine (8.16 g, 87% yield) as a white solid. It was used in the next step without purification. After stirring for 4 h at room temperature the layers were separated The organic layer was washed with water dried over MgSO4 filtered The solvent was removed in vacuo
来源 ID: ord-7aa16512fe6d405aa32028c1a7a3ebf4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d03357266a1f4b39971c556edc2dc47f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a suspension of 10% palladium on carbon (0.2 g) in 30 mL of ethyl alcohol was added a solution of 1-benzyl-4-benzamido-piperidine (0.5 g, 1.79 mmol) in ethyl alcohol (10 mL). The resulting suspension was hydrogenated at 100 psi at 50° C. for 30 h after which it was filtered through a pad of celite and the solvent was removed in vacuo to obtain 0.34 g (100%) of 4-benzamidopiperidine as a white solid. It was used in the next step without purification. after which it was filtered through a pad of celite the solvent was removed in vacuo
来源 ID: ord-2f29796371034863a69c1bad23542458反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a biphasic solution of 4-amino-1-benzylpiperidine (6.0 g, 31.6 mmol), K2CO3 (8.71 g, 63.1 mmol) in CH2Cl2 (200 mL) and water (100 mL) was added benzoyl chloride (4.86 g, 34.7 mmol) in 20 mL of CH2Cl2 at 0° C. with stirring. After stirring for 4 h at room temperature, the layers were separated. The organic layer was washed with water, dried over MgSO4 and filtered. The solvent was removed in vacuo to obtain 1-benzyl-4-benzamidopiperidine (8.16 g, 87% yield) as a white solid. It was used in the next step without purification. After stirring for 4 h at room temperature the layers were separated The organic layer was washed with water dried over MgSO4 filtered The solvent was removed in vacuo
来源 ID: ord-7aa16512fe6d405aa32028c1a7a3ebf4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d03357266a1f4b39971c556edc2dc47fPubChem 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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