反应 #4161784
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-7c49b668b8f441e2be759c4a9f361e08暂无可渲染的结构数据
C1=C(C=C(C=C1Cl)Cl)NN产品信息
3,5-二氯苯肼(CAS 39943-56-1)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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合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7c49b668b8f441e2be759c4a9f361e08反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f2665fcba64e4871a9e8cd58d74dabeb反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-7c49b668b8f441e2be759c4a9f361e08反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone. evaporate in vacuo to obtain a residue Separate the layers extract the aqueous layer with ethyl acetate dry over MgSO4 filter evaporate in vacuo
来源 ID: ord-2d1ace39198441088307ced858ae1bb0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone. evaporate in vacuo to obtain a residue Separate the layers extract the aqueous layer with ethyl acetate dry over MgSO4 filter evaporate in vacuo
来源 ID: ord-2d1ace39198441088307ced858ae1bb0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone. evaporate in vacuo to obtain a residue Separate the layers extract the aqueous layer with ethyl acetate dry over MgSO4 filter evaporate in vacuo
来源 ID: ord-d5e34066087a4da88c2fe42ecfd555ff反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone. evaporate in vacuo to obtain a residue Separate the layers extract the aqueous layer with ethyl acetate dry over MgSO4 filter evaporate in vacuo
来源 ID: ord-cbc1d41875ea43ab9b0395657970d370反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone. evaporate in vacuo to obtain a residue Separate the layers extract the aqueous layer with ethyl acetate dry over MgSO4 filter evaporate in vacuo
来源 ID: ord-ce8140f302344c27b81a28d9e0b9b7d7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone. evaporate in vacuo to obtain a residue Separate the layers extract the aqueous layer with ethyl acetate dry over MgSO4 filter evaporate in vacuo
来源 ID: ord-ce8140f302344c27b81a28d9e0b9b7d7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f2665fcba64e4871a9e8cd58d74dabeb反应条件: temp:180.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 1,3,5-trichlorobenzene (2.53 g), hydrazine hydrate (3.48 g, 5 molar equivalents) and pyridine (12 ml) was heated in an autoclave (purged with argon) for 6 hours at 180° C. The mixture was cooled, the excess hydrazine decanted and the organic phase evaporated in vacuo to give the title compound in 60% yield. It was shown that 65% of the starting material had been consumed, thus indicating that the reaction had occurred with high selectivity. The mixture was cooled the excess hydrazine decanted the organic phase evaporated in vacuo
来源 ID: ord-3e6a2dccd2424f91bb0356d383f5ee0e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Combine 3,5-dichlorophenylhydrazine (300 g) and ethanol (2 L). Add ethyl pyruvate (153.6 mL) and sulfuric acid (25 mL). After 3 hours, evaporate in vacuo to obtain a residue. Cover the residue with ethyl acetate and water. Add solid sodium bicarbonate until the aqueous layer is neutralized. Separate the layers and extract the aqueous layer with ethyl acetate. Combine the organic layers, dry over MgSO4, filter, and evaporate in vacuo to give ethyl pyruvate-3,5-dichlorophenylhydrazone. evaporate in vacuo to obtain a residue Separate the layers extract the aqueous layer with ethyl acetate dry over MgSO4 filter evaporate in vacuo
来源 ID: ord-010acf663e2d44aa8dbe736c872f676fPubChem References
以下资料来自该化合物的公开数据库参考记录。
