反应 #4163609
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-43a8b6fc6d2d424ab73d1cfd66c92311暂无可渲染的结构数据
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3-溴乙酰苯胺(CAS 621-38-5)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-43a8b6fc6d2d424ab73d1cfd66c92311反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-816f3f6643bf4b4a8fe6587afc453a44反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a31349d623694a49aa181b27b2b9c90f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c1e95ec78bfa4b06904dc3fafd66fc60反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9dd06a3aeed64b4d8ba2ea4fe7dbab1b反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-110661fada1a40b69ff93267927e0650反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-43a8b6fc6d2d424ab73d1cfd66c92311反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-816f3f6643bf4b4a8fe6587afc453a44反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-816f3f6643bf4b4a8fe6587afc453a44反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In a manner similar to that of Example (27b), by reaction of 820 mg (20.5 mmol, 1.1 eq) of 60% sodium hydride, 4.0 g (18.7 mmol, 1 eq) of N-(3-bromophenyl)acetamide (prepared in Example 27a) and 2.20 mL (22.4 mmol, 1.2 eq) of 1-iodopropane in 15 ml of tetrahydrofuran in the presence of 1.5 ml of dimethylformamide, N-(3-bromophenyl)-N-propylacetamide is obtained in oil form and is used in the following reaction without further purification.
来源 ID: ord-b8c72420ab1243119e5a952cb08513ba反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In a manner similar to that of Example (27b), by reaction of 820 mg (20.5 mmol, 1.1 eq) of 60% sodium hydride, 4.0 g (18.7 mmol, 1 eq) of N-(3-bromophenyl)acetamide (prepared in Example 27a) and 2.20 mL (22.4 mmol, 1.2 eq) of 1-iodopropane in 15 ml of tetrahydrofuran in the presence of 1.5 ml of dimethylformamide, N-(3-bromophenyl)-N-propylacetamide is obtained in oil form and is used in the following reaction without further purification.
来源 ID: ord-b8c72420ab1243119e5a952cb08513ba反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 820 mg (20.5 mmol, 1.1 eq) of 60% sodium hydride are added to a solution of 4.0 g (18.7 mmol, 1 eq) of N-(3-bromophenyl)acetamide and 1.80 mL (22.4 mmol, 1.2 eq) of ethyl iodide in 15 ml of tetrahydrofuran in the presence of 1.5 ml of dimethylformamide. The reaction medium is stirred at room temperature for 12 hours and then hydrolyzed with water and extracted with ethyl acetate. The organic phases are combined, washed with sodium chloride solution and dried over sodium sulfate. The solvents are evaporated off and the N-(3-bromophenyl)-N-ethylacetamide obtained in oil form is used in the following reaction without further purification. hydrolyzed with water and extracted with ethyl acetate washed with sodium chloride solution dried over sodium sulfate The solvents are evaporated off
来源 ID: ord-0f32b78ee59147788d54de37ff1276ddPubChem References
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