反应 #4127058
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-cade1a4ee3c64696abeda83e051692da暂无可渲染的结构数据
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7 条反应 · 7 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cade1a4ee3c64696abeda83e051692da反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e7592f2e3458437683ed3542990fb166反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 25 g of K2CO3 are added to a solution of 20 g of phenylhydrazine hydrochloride in 150 ml of methyl formate and 60 ml of water, and the mixture is refluxed for 1 hour and left at AT for 12 hours with stirring. The precipitate formed is filter-dried, and washed with a propan-2-ol/petroleum ether mixture. 18.8 g of the expected compound are obtained. the mixture is refluxed for 1 hour The precipitate formed is filter-dried washed with a propan-2-ol/petroleum ether mixture
来源 ID: ord-bac0b619a90d406c8fea04ff37237830反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-cade1a4ee3c64696abeda83e051692da反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of N'-phenylformohydrazide (20.59 g) in dry tetrahydrofuran (750 ml) was added dropwise under nitrogen to a stirred suspension of lithium aluminium hydride (10 g) in dry tetrahydrofuran (200 ml), then the mixture was stirred and heated under reflux for 4 hours. The mixture was quenched by the slow dropwise addition of water (10 ml), followed by 5M aqueous sodium hydroxide solution (10 ml), then water (20 ml), then it was filtered, dried (MgSO4) and the solvent removed in vacuo to yield an oil. The oil was dissolved in ether, redried (MgSO4) and the solvent removed in vacuo to yield 1-methyl-2-phenylhydrazine (14.1 g) as a yellow oil. heated under reflux for 4 hours The mixture was quenched by the slow dropwise addition of water (10 ml) water (20 ml), then it was filtered dried (MgSO4) the solvent removed in vacuo to yield an oil redried (MgSO4) the solvent removed in vacuo
来源 ID: ord-b7104568c8a149abbeed6e3faddea091反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phenylhydrazine (75 g) was added dropwise at <20° C. to stirred acetic acid (198 ml). When the addition was complete, formamide (27.9 ml) was added in one portion, and the mixture was stirred at ambient temperature for 4 hours. Water (225 ml) was added, and the resulting solid was collected by filtration, washed well with water, and dried in vacuo to give N'-phenylformohydrazide (68.8 g) as a cream solid, m.p. 138-143° C. When the addition the resulting solid was collected by filtration washed well with water dried in vacuo
来源 ID: ord-a9577aca3c3546ab9215bcbcaafc12a3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 25 g of K2CO3 are added to a solution of 20 g of phenylhydrazine hydrochloride in 150 ml of methyl formate and 60 ml of water, and the mixture is refluxed for 1 hour and left at AT for 12 hours with stirring. The precipitate formed is filter-dried, and washed with a propan-2-ol/petroleum ether mixture. 18.8 g of the expected compound are obtained. the mixture is refluxed for 1 hour The precipitate formed is filter-dried washed with a propan-2-ol/petroleum ether mixture
来源 ID: ord-bac0b619a90d406c8fea04ff37237830PubChem References
以下资料来自该化合物的公开数据库参考记录。
