反应 #4056054
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-6458dd35d56940f4b2b74fa51f5f4995暂无可渲染的结构数据
CCCCC(=O)NC1=CC=CC(=C1)N产品信息
N-(3-氨基苯基)戊酰胺(CAS 59683-84-0)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 5138852
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
8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6458dd35d56940f4b2b74fa51f5f4995反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 42 g of diketene were added to a mixture of 96 g of m-aminovaleranilide in 400 ml of benzene and the mixture was stirred for 16 hours at 20° C. The benzene was decanted and the residue was added to refluxing benzene. The mixture was treated with activated carbon and filtered to obtain raw m-valeramido-acetylacetanilide melting at 90° C. Crystallization from ethyl acetate yielded 34 g of pure m-valeramido-acetylacetanilide melting at 116° C. The benzene was decanted the residue was added to refluxing benzene The mixture was treated with activated carbon filtered to obtain raw m-valeramido-acetylacetanilide melting at 90° C Crystallization from ethyl acetate
来源 ID: ord-8d826342c94249ddbeca380895b4516c反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 42 g of diketene were added to a mixture of 96 g of m-aminovaleranilide in 400 ml of benzene and the mixture was stirred for 16 hours at 20° C. The benzene was decanted and the residue was added to refluxing benzene. The mixture was treated with activated carbon and filtered to obtain raw m-valeramido-acetylacetanilide melting at 90° C. Crystallization from ethyl acetate yielded 34 g of pure m-valeramido-acetylacetanilide melting at 116° C. The benzene was decanted the residue was added to refluxing benzene The mixture was treated with activated carbon filtered to obtain raw m-valeramido-acetylacetanilide melting at 90° C Crystallization from ethyl acetate
来源 ID: ord-8d826342c94249ddbeca380895b4516c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 177.6 g of m-nitrovaleranilide, 160 ml of water, 8 ml of 22° Be hydrochloric acid and 640 ml of 95% ethanol was refluxed and 480 g of iron powder were added with stirring over 30 minutes. Reflux was continued for 30 minutes with stirring and the mixture was filtered. The filtrate was concentrated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with an 8- 2 methylene chloride-acetone mixture gave 151 g of m-aminovaleranilide with a specific rotation nD20 = 1.541. was refluxed Reflux was continued for 30 minutes with stirring the mixture was filtered The filtrate was concentrated to dryness under reduced pressure the residue was chromatographed over silica gel Elution with an 8- 2 methylene chloride-acetone mixture
来源 ID: ord-ca9d615e62c84de4b4aad95201a98513反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 177.6 g of m-nitrovaleranilide, 160 ml of water, 8 ml of 22° Be hydrochloric acid and 640 ml of 95% ethanol was refluxed and 480 g of iron powder were added with stirring over 30 minutes. Reflux was continued for 30 minutes with stirring and the mixture was filtered. The filtrate was concentrated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with an 8- 2 methylene chloride-acetone mixture gave 151 g of m-aminovaleranilide with a specific rotation nD20 = 1.541. was refluxed Reflux was continued for 30 minutes with stirring the mixture was filtered The filtrate was concentrated to dryness under reduced pressure the residue was chromatographed over silica gel Elution with an 8- 2 methylene chloride-acetone mixture
来源 ID: ord-ca9d615e62c84de4b4aad95201a98513反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6458dd35d56940f4b2b74fa51f5f4995反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 42 g of diketene were added to a mixture of 96 g of m-aminovaleranilide in 400 ml of benzene and the mixture was stirred for 16 hours at 20° C. The benzene was decanted and the residue was added to refluxing benzene. The mixture was treated with activated carbon and filtered to obtain raw m-valeramido-acetylacetanilide melting at 90° C. Crystallization from ethyl acetate yielded 34 g of pure m-valeramido-acetylacetanilide melting at 116° C. The benzene was decanted the residue was added to refluxing benzene The mixture was treated with activated carbon filtered to obtain raw m-valeramido-acetylacetanilide melting at 90° C Crystallization from ethyl acetate
来源 ID: ord-8d826342c94249ddbeca380895b4516c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 177.6 g of m-nitrovaleranilide, 160 ml of water, 8 ml of 22° Be hydrochloric acid and 640 ml of 95% ethanol was refluxed and 480 g of iron powder were added with stirring over 30 minutes. Reflux was continued for 30 minutes with stirring and the mixture was filtered. The filtrate was concentrated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with an 8- 2 methylene chloride-acetone mixture gave 151 g of m-aminovaleranilide with a specific rotation nD20 = 1.541. was refluxed Reflux was continued for 30 minutes with stirring the mixture was filtered The filtrate was concentrated to dryness under reduced pressure the residue was chromatographed over silica gel Elution with an 8- 2 methylene chloride-acetone mixture
来源 ID: ord-ca9d615e62c84de4b4aad95201a98513PubChem References
以下资料来自该化合物的公开数据库参考记录。
