反应 #4157957
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-8b0d3b76c5d949e29497764cce420e2a暂无可渲染的结构数据
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3-(氯甲氧基)丙-1-炔(CAS 40308-66-5)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-8b0d3b76c5d949e29497764cce420e2a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e27cea3db06e47b0a9d514c8d5ac589f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-928edf10e5af46e7a697292bb89bfe29反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8b0d3b76c5d949e29497764cce420e2a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 0.6 g of N-methoxybenzenesulfonamide was dissolved in 10 ml of acetonitrile, and 0.44 g of potassium carbonate and 0.34 g of chloromethylpropargyl ether were added thereto in this order. The mixture was stirred at room temperature for 4 hours. After completion of the reaction, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was dried, concentrated, and purified by silica gel column chromatography to obtain 0.7 g of N-methoxy-N-propargyloxymethylbenzenesulfonamide. was added to the reaction solution the mixture was extracted with ethyl acetate The extract was dried concentrated purified by silica gel column chromatography
来源 ID: ord-8a7f1a41a70a4d3db418869aba312fea反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 0.6 g of N-methoxybenzamide was dissolved in 10 ml of acetonitrile, and 0.55 g of potassium carbonate and 0.42 g of chloromethylpropargyl ether were added thereto in this order. The mixture was stirred at room temperature for 3 hours. After completion of the reaction, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was dried, concentrated and purified by silica gel column chromatography to obtain 0.8 g of N-methoxy-N-propargyloxymethylbenzamide. was added to the reaction solution the mixture was extracted with ethyl acetate The extract was dried concentrated purified by silica gel column chromatography
来源 ID: ord-78a2d25f14b9434b93e8ef7743620d47反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 0.37 g of sodium hydride (60% in oil) was suspended in 10 ml of tetrahydrofuran, and 0.8 g of methyl N-methoxycarbamate and 0.96 g of chloromethylpropargyl ether were added thereto in this order while being cooled with ice. The mixture was heat-refluxed for 1 hour. After completion of the reaction, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was dried, concentrated and purified by silica gel column chromatography to obtain 1.0 g of methyl N-methoxy-N-propargyloxymethylcarbamate. in this order while being cooled with ice The mixture was heat-refluxed for 1 hour was added to the reaction solution the mixture was extracted with ethyl acetate The extract was dried concentrated purified by silica gel column chromatography
来源 ID: ord-b317ab1e31f1484d8c7fa6fc2ad9a7be反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e27cea3db06e47b0a9d514c8d5ac589f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-928edf10e5af46e7a697292bb89bfe29反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 0.6 g of N-methoxybenzenesulfonamide was dissolved in 10 ml of acetonitrile, and 0.44 g of potassium carbonate and 0.34 g of chloromethylpropargyl ether were added thereto in this order. The mixture was stirred at room temperature for 4 hours. After completion of the reaction, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was dried, concentrated, and purified by silica gel column chromatography to obtain 0.7 g of N-methoxy-N-propargyloxymethylbenzenesulfonamide. was added to the reaction solution the mixture was extracted with ethyl acetate The extract was dried concentrated purified by silica gel column chromatography
来源 ID: ord-8a7f1a41a70a4d3db418869aba312fea反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 0.6 g of N-methoxybenzamide was dissolved in 10 ml of acetonitrile, and 0.55 g of potassium carbonate and 0.42 g of chloromethylpropargyl ether were added thereto in this order. The mixture was stirred at room temperature for 3 hours. After completion of the reaction, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was dried, concentrated and purified by silica gel column chromatography to obtain 0.8 g of N-methoxy-N-propargyloxymethylbenzamide. was added to the reaction solution the mixture was extracted with ethyl acetate The extract was dried concentrated purified by silica gel column chromatography
来源 ID: ord-78a2d25f14b9434b93e8ef7743620d47反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 0.37 g of sodium hydride (60% in oil) was suspended in 10 ml of tetrahydrofuran, and 0.8 g of methyl N-methoxycarbamate and 0.96 g of chloromethylpropargyl ether were added thereto in this order while being cooled with ice. The mixture was heat-refluxed for 1 hour. After completion of the reaction, water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was dried, concentrated and purified by silica gel column chromatography to obtain 1.0 g of methyl N-methoxy-N-propargyloxymethylcarbamate. in this order while being cooled with ice The mixture was heat-refluxed for 1 hour was added to the reaction solution the mixture was extracted with ethyl acetate The extract was dried concentrated purified by silica gel column chromatography
来源 ID: ord-b317ab1e31f1484d8c7fa6fc2ad9a7bePubChem References
以下资料来自该化合物的公开数据库参考记录。
