反应 #4161179
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-69fae400863a4e77b6526e05504b9df9暂无可渲染的结构数据
N(CCCCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCCCC产品信息
N-十八烷基十八烷-1-胺(CAS 112-99-2)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。
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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-69fae400863a4e77b6526e05504b9df9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a19087e09abe4f6dab0d9e4edd0ac213反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1f52e4cfbfb34d7f86fd37a1c5a1e056反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9dce3401bc1e4f12ae731f4bd7712921反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 1-chloro-2,4-dinitrobenzene (Aldrich, 2.02 g, 10 mmol), sodium carbonate (1.27 g, 12 mmol), dioctadecylamine (Pfaltz & Bauer, 6.26 g, 12 mmol) and dry dimethylformamide (10 mL) was heated to 80°-90° C. under a nitrogen atmosphere for 1 h. The cooled mixture was diluted with water and extracted with ether. The extracts were washed with water and dried over magnesium sulfate. The solvent was removed and the solid recrystallized to give N,N-dioctadecyl-2,4-dinitrobenzenamine (6.0 g, 87%): mp 55.5°-57.5° C. was heated to 80°-90° C. under a nitrogen atmosphere for 1 h extracted with ether The extracts were washed with water dried over magnesium sulfate The solvent was removed the solid recrystallized
来源 ID: ord-c452d77aca5c4d06a3732c571f03370d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Dioctadecylamine (26.0 g., 0.05 M), α-bromo-p-tolunitrile (4.9 g., 0.025 M) and chloroform (500 ml.) are stirred at room temperature for 24 hours. The precipitate of dioctadecylamine hydrobromide is filtered off and the filtrate concentrated under reduced pressure. The residue is slurried in methanol, filtered, and evaporated to give 1-(dioctadecylamino)methyl-4-cyanobenzene (15.5 g., 97.5% yield). The precipitate of dioctadecylamine hydrobromide is filtered off the filtrate concentrated under reduced pressure filtered evaporated
来源 ID: ord-64cf9590b0c44688a80e1dd74c45498d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of dioctadecylamine (5.2 g., 0.01 mole), ethyl 4-bromobutyrate (1.95 g., 0.01 mole) and toluene (50 ml.) is heated at reflux for sixteen hours, then cooled and concentrated in vacuo to a semi-solid oil. The oil is triturated with ethylacetate, filtered, and the filtrate washed with water, then dried (Na2SO4). Removal of the solvent gives the product as an oil (3.7 g.). at reflux for sixteen hours cooled concentrated in vacuo to a semi-solid oil The oil is triturated with ethylacetate filtered the filtrate washed with water dried (Na2SO4) Removal of the solvent
来源 ID: ord-c21445e40754415299c7d97e6aa8a6ec反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-(Dioctadecylamino)propionitrile is prepared by refluxing a mixture of dioctadecylamine (200 g.) and acrylonitrile (1903.8 ml.) for eighteen hours. The mixture is then concentrated to a waxy semi-solid which is slurried in acetone, filtered, and air dried overnight. by refluxing The mixture is then concentrated to a waxy semi-solid which filtered air dried overnight
来源 ID: ord-4e784c4e26e14199b4fb1e5dd57e98b0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 1-chloro-2,4-dinitrobenzene (Aldrich, 2.02 g, 10 mmol), sodium carbonate (1.27 g, 12 mmol), dioctadecylamine (Pfaltz & Bauer, 6.26 g, 12 mmol) and dry dimethylformamide (10 mL) was heated to 80°-90° C. under a nitrogen atmosphere for 1 h. The cooled mixture was diluted with water and extracted with ether. The extracts were washed with water and dried over magnesium sulfate. The solvent was removed and the solid recrystallized to give N,N-dioctadecyl-2,4-dinitrobenzenamine (6.0 g, 87%): mp 55.5°-57.5° C. was heated to 80°-90° C. under a nitrogen atmosphere for 1 h extracted with ether The extracts were washed with water dried over magnesium sulfate The solvent was removed the solid recrystallized
来源 ID: ord-a15df1bda77d4085a55925ed4136bd61反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 1-chloro-2,4-dinitrobenzene (Aldrich, 2.02 g, 10 mmol), sodium carbonate (1.27 g, 12 mmol), dioctadecylamine (Pfaltz & Bauer, 6.26 g, 12 mmol) and dry dimethylformamide (10 mL) was heated to 80°-90° C. under a nitrogen atmosphere for 1 h. The cooled mixture was diluted with water and extracted with ether. The extracts were washed with water and dried over magnesium sulfate. The solvent was removed and the solid recrystallized to give N,N-dioctadecyl-2,4-dinitrobenzenamine (6.0 g, 87%): mp 55.5°-57.5° C. was heated to 80°-90° C. under a nitrogen atmosphere for 1 h extracted with ether The extracts were washed with water dried over magnesium sulfate The solvent was removed the solid recrystallized
来源 ID: ord-2079cff997264068a9d3a4b8bdb2f8d7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-69fae400863a4e77b6526e05504b9df9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Dioctadecylamine (26.0 g., 0.05 M), α-bromo-p-tolunitrile (4.9 g., 0.025 M) and chloroform (500 ml.) are stirred at room temperature for 24 hours. The precipitate of dioctadecylamine hydrobromide is filtered off and the filtrate concentrated under reduced pressure. The residue is slurried in methanol, filtered, and evaporated to give 1-(dioctadecylamino)methyl-4-cyanobenzene (15.5 g., 97.5% yield). The precipitate of dioctadecylamine hydrobromide is filtered off the filtrate concentrated under reduced pressure filtered evaporated
来源 ID: ord-6826c80fe9a447d7a2fe14cc7d63ee82PubChem References
以下资料来自该化合物的公开数据库参考记录。
