反应 #4109869
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-f0cc967e6e164ebc9203fcd54b90713d暂无可渲染的结构数据
C1=COC(=C1)C(=O)C#N产品信息
2-呋喃基GLY氧基O腈(CAS 6047-91-2)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 80147
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
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f0cc967e6e164ebc9203fcd54b90713d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The 24.5 g. of crude 2-furoylcyanide was mixed with 160 ml. concentrated hydrochloric acid at 25° C. with intermittent stirring. The reaction was stored for 24 hours at 25° C. and diluted with 80 ml. of water. The reaction was stirred for 5 minutes and filtered. The filtrate was saturated with sodium chloride and extracted with 5 × 120 ml. of 1:1 ether-ethyl acetate solution. The extracts were combined, dried over anhydrous magnesium sulfate and evaporated at 30° C. (15 mm.) to give a brownish-orange solid. The solid was dissolved in methanol, treated with charcoal and evaporated under reduced pressure (15 mm.) to dryness to yield 17 g. of the acid. at 25° C. diluted with 80 ml filtered extracted with 5 × 120 ml dried over anhydrous magnesium sulfate evaporated at 30° C. (15 mm.) to give a brownish-orange solid evaporated under reduced pressure (15 mm.) to dryness to yield 17 g
来源 ID: ord-494c4bfeb54d4c40b5487c58afdd4457反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f0cc967e6e164ebc9203fcd54b90713d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The 24.5 g. of crude 2-furoylcyanide was mixed with 160 ml. concentrated hydrochloric acid at 25° C. with intermittent stirring. The reaction was stored for 24 hours at 25° C. and diluted with 80 ml. of water. The reaction was stirred for 5 minutes and filtered. The filtrate was saturated with sodium chloride and extracted with 5 × 120 ml. of 1:1 ether-ethyl acetate solution. The extracts were combined, dried over anhydrous magnesium sulfate and evaporated at 30° C. (15 mm.) to give a brownish-orange solid. The solid was dissolved in methanol, treated with charcoal and evaporated under reduced pressure (15 mm.) to dryness to yield 17 g. of the acid. at 25° C. diluted with 80 ml filtered extracted with 5 × 120 ml dried over anhydrous magnesium sulfate evaporated at 30° C. (15 mm.) to give a brownish-orange solid evaporated under reduced pressure (15 mm.) to dryness to yield 17 g
来源 ID: ord-b07a481c2b874598a273772225e601fe反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The 24.5 g. of crude 2-furoylcyanide was mixed with 160 ml. concentrated hydrochloric acid at 25° C. with intermittent stirring. The reaction was stored for 24 hours at 25° C. and diluted with 80 ml. of water. The reaction was stirred for 5 minutes and filtered. The filtrate was saturated with sodium chloride and extracted with 5×120 ml. of 1:1 ether-ethyl acetate solution. The extracts were combined, dried over anhydrous magnesium sulfate and evaporated at 30° C. (15 mm.) to give a brownish-orange solid. The solid was dissolved in methanol, treated with charcoal and evaporated under reduced pressure (15 mm.) to dryness to yield 17 g. of the acid. at 25° C. diluted with 80 ml filtered extracted with 5×120 ml dried over anhydrous magnesium sulfate evaporated at 30° C. (15 mm.) to give a brownish-orange solid evaporated under reduced pressure (15 mm.) to dryness to yield 17 g
来源 ID: ord-531f3ac0317542b1a88bbda08ac4d533反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The 24.5 g. of crude 2-furoylcyanide was mixed with 160 ml. concentrated hydrochloric acid at 25° C. with intermittent stirring. The reaction was stored for 24 hours at 25° C. and diluted with 80 ml. of water. The reaction was stirred for 5 minutes and filtered. The filtrate was saturated with sodium chloride and extracted with 5 × 120 ml. of 1:1 ether-ethyl acetate solution. The extracts were combined, dried over anhydrous magnesium sulfate and evaporated at 30° C. (15 mm.) to give a brownish-orange solid. The solid was dissolved in methanol, treated with charcoal and evaporated under reduced pressure (15 mm.) to dryness to yield 17 g. of the acid. at 25° C. diluted with 80 ml filtered extracted with 5 × 120 ml dried over anhydrous magnesium sulfate evaporated at 30° C. (15 mm.) to give a brownish-orange solid evaporated under reduced pressure (15 mm.) to dryness to yield 17 g
来源 ID: ord-494c4bfeb54d4c40b5487c58afdd4457PubChem References
以下资料来自该化合物的公开数据库参考记录。
