反应 #3871738
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-b8d28c5ff9e74c7c994de7c1dbf06579暂无可渲染的结构数据
CCCN1C(=O)C2=CC=CC=C2C1=O产品信息
N-丙基酞酰亚胺(CAS 5323-50-2)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 79215
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-b8d28c5ff9e74c7c994de7c1dbf06579反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-82e956f562c045cc82e4152d0cfed6f0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-propylphthalimide (50 g) was nitrated in 500 g 99% nitric acid to produce 4-nitro-N-propylphthalimide under conditions described in Example 2.
来源 ID: ord-dbe1a8386e7b4f7ab0a4eb9fa8f9419a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-propylphthalimide (50 g) was nitrated in 500 g 99% nitric acid to produce 4-nitro-N-propylphthalimide under conditions described in Example 2.
来源 ID: ord-dbe1a8386e7b4f7ab0a4eb9fa8f9419a反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-Hydroxy-2-propyl-2,3-dihydroisoindol-1-one is prepared as described in Example 1, starting with 1.5 g of N-propylphthalimide in 25 cm3 of methanol and 0.48 g of potassium borohydride. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours and is then cooled to a temperature in the region of 0° C. and distilled water is added dropwise. The methanol is then partially evaporated off under reduced pressure (2 kPa) at a temperature in the region of 35° C. and the residue is cooled to 0° C. The precipitate obtained is filtered off and then washed with cold water. The solid is taken up in dichloromethane and the solvent is then evaporated to dryness under reduced pressure (2 kPa) at a temperature in the region of 35° C. 1.0 g of 3-hydroxy-2-propyl-2,3-dihydroisoindol-1-one is thus obtained in the form of a beige-colored powder. (Rf=0.6, thin layer chromatography on silica gel, eluent: cyclohexane/ethyl acetate (30/70 by volume)). 3-Hydroxy-2-propyl-2,3-dihydroisoindol-1-one is prepared is then cooled to a temperature in the region of 0° C. distilled water is added dropwise The methanol is then partially evaporated off under reduced pressure (2 kPa) at a temperature in the region of 35° C. the residue is cooled to 0° C The precipitate obtained is filtered off washed with cold water the solvent is then evaporated to dryness under reduced pressure (2 kPa) at a temperature in the region of 35° C
来源 ID: ord-d2087421d4314cd886e68a6d22f2b0c1反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-propylphthalimide (50 g) was nitrated in 500 g 99% nitric acid to produce 4-nitro-N-propylphthalimide under conditions described in Example 2.
来源 ID: ord-87b4481cac9d4fa8bf3111f1b75b17da反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-propylphthalimide (50 g) was nitrated in 500 g 99% nitric acid to produce 4-nitro-N-propylphthalimide under conditions described in Example 2.
来源 ID: ord-87b4481cac9d4fa8bf3111f1b75b17da反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-82e956f562c045cc82e4152d0cfed6f0反应条件: temp:20.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-Hydroxy-2-propyl-2,3-dihydroisoindol-1-one is prepared as described in Example 1, starting with 1.5 g of N-propylphthalimide in 25 cm3 of methanol and 0.48 g of potassium borohydride. The reaction mixture is stirred at a temperature in the region of 20° C. for 20 hours and is then cooled to a temperature in the region of 0° C. and distilled water is added dropwise. The methanol is then partially evaporated off under reduced pressure (2 kPa) at a temperature in the region of 35° C. and the residue is cooled to 0° C. The precipitate obtained is filtered off and then washed with cold water. The solid is taken up in dichloromethane and the solvent is then evaporated to dryness under reduced pressure (2 kPa) at a temperature in the region of 35° C. 1.0 g of 3-hydroxy-2propyl-2,3-dihydroisoindol-1-one is thus obtained in the form of a beige-colored powder. (Rf=0.6, thin layer chromatography on silica gel, eluent: cyclohexane/ethyl acetate (30/70 by volume)). 3-Hydroxy-2-propyl-2,3-dihydroisoindol-1-one is prepared is then cooled to a temperature in the region of 0° C. distilled water is added dropwise The methanol is then partially evaporated off under reduced pressure (2 kPa) at a temperature in the region of 35° C. the residue is cooled to 0° C The precipitate obtained is filtered off washed with cold water the solvent is then evaporated to dryness under reduced pressure (2 kPa) at a temperature in the region of 35° C
来源 ID: ord-b899b9d8d8054722b2f738da334d7782反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-propylphthalimide (50 g) was nitrated in 500 g 99% nitric acid to produce 4-nitro-N-propylph thalimide under conditions described in Example 2.
来源 ID: ord-f29dc1bdf89e4686be90cda2f9cefc30反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-propylphthalimide (50 g) was nitrated in 500 g 99% nitric acid to produce 4-nitro-N-propylphthalimide under conditions described in Example 2.
来源 ID: ord-55ab1d31b0dc491e8d89341bdd49a9b4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-propylphthalimide (50 g) was nitrated in 500 g 99% nitric acid to produce 4-nitro-N-propylphthalimide under conditions described in Example 2.
来源 ID: ord-dbe1a8386e7b4f7ab0a4eb9fa8f9419aPubChem References
以下资料来自该化合物的公开数据库参考记录。
