反应 #3862114
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-b479acb552034d01b197d963c532f7a4暂无可渲染的结构数据
C1=COC(=C1)CNC(=O)CCl产品信息
2-氯-N-呋喃甲基乙酰胺(CAS 40914-13-4)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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9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b479acb552034d01b197d963c532f7a4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, additional funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwise so that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, additional funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-dfd57f5b61284c5bb698f76d5a2e50f4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, additional funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwise so that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, additional funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-dfd57f5b61284c5bb698f76d5a2e50f4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, addition funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwise so that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, addition funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-579f141a799349e98a55b521e785a4e5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, addition funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwise so that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, addition funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-579f141a799349e98a55b521e785a4e5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, additional funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwise so that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, additional funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-dfd57f5b61284c5bb698f76d5a2e50f4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, addition funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwiseso that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, addition funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-5bde5c864fc84686a5c88f89ebfe68fd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, addition funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwise so that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, addition funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-579f141a799349e98a55b521e785a4e5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-Furfurylchloroacetamide was prepared by adding 20.0 g. (0.206 mole) furfuryl amine in sufficient toluene to make a 15% solution to a 500 ml. three neck round bottom flask equipped with magnetic stir bar, additional funnel, and cooling bath and then adding 36 ml. of 20% sodium hydroxide. The mixture was cooled to 0°-5° C. and chloroacetyl chloride was added dropwise so that the reaction temperature was maintained at 5°-10° C. After the addition, a solid deposited on the walls of the flask. It was recrystallized from ether as a light tan solid. Yield was 85%. by adding 20.0 g three neck round bottom flask equipped with magnetic stir bar, additional funnel cooling bath adding 36 ml The mixture was cooled to 0°-5° C. was maintained at 5°-10° C After the addition It was recrystallized from ether as a light tan solid
来源 ID: ord-dfd57f5b61284c5bb698f76d5a2e50f4PubChem References
以下资料来自该化合物的公开数据库参考记录。
