反应 #4136516
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-0efd9bf8b2d6474aa982b9a4c8e54c22暂无可渲染的结构数据
CNCC1=CC=C(C=C1)F产品信息
N-甲基-4-氟苄胺(CAS 405-66-3)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-0efd9bf8b2d6474aa982b9a4c8e54c22反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ef1a6af2c2044e9a857ae36f4156b58c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-703b43fe96674b41b85974abe83f0bb3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4e298bb6207b4791bf4f6610418bcd6d反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-85046a86571f459689fd6ca3fd10e196反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-03305bda11ac47c1855109958cadeafe反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0efd9bf8b2d6474aa982b9a4c8e54c22反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0efd9bf8b2d6474aa982b9a4c8e54c22反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 17.1 g (0.14 mol) of N-acetyl-4-piperidone and 16.9 g (0.14 mol) of N-(4-fluorobenzyl)-N-methylamine were reacted in a similar manner to Preparation 6. 25.1 g of 1-acetyl-4-(N-(4-fluorobenzyl)-N-methylamino)piperidine were obtained.
来源 ID: ord-b08d88381dd14505a7c8299a43546274反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 17.1 g (0.14 mol) of N-acetyl-4-piperidone and 16.9 g (0.14 mol) of N-(4-fluorobenzyl)-N-methylamine were reacted in a similar manner to Preparation 6. 25.1 g of 1-acetyl-4-(N-(4-fluorobenzyl)-N-methylamino)piperidine were obtained.
来源 ID: ord-b08d88381dd14505a7c8299a43546274反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This compound was prepared from 4-Fluoro-N-methylbenzylamine which in turn was prepared from 4-Fluoro-N-methylbenzamide. Practical details are as follows: 4-Fluorobenzoyl chloride (25g) was added dropwise to a stirred aqueous solution of methylamine (40% w/v; 250 ml) at 0° C. over 30 min. The mixture was stirred for 12 h at room temperature, concentrated to half volume and the resulting crystalline precipitate was collected and recrystallized from water to furnish the N-methylbenzamide as colourless needles, (24.1 g; 89.1%), m.p. 131°-132° C. concentrated to half volume the resulting crystalline precipitate was collected recrystallized from water
来源 ID: ord-afdb13066def4d9cbbc7a209980b998e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This compound was prepared from 4-Fluoro-N-methylbenzylamine which in turn was prepared from 4-Fluoro-N-methylbenzamide. Practical details are as follows: 4-Fluorobenzoyl chloride (25g) was added dropwise to a stirred aqueous solution of methylamine (40% w/v; 250 ml) at 0° C. over 30 min. The mixture was stirred for 12 h at room temperature, concentrated to half volume and the resulting crystalline precipitate was collected and recrystallized from water to furnish the N-methylbenzamide as colourless needles, (24.1 g; 89.1%), m.p. 131°-132° C. concentrated to half volume the resulting crystalline precipitate was collected recrystallized from water
来源 ID: ord-afdb13066def4d9cbbc7a209980b998ePubChem References
以下资料来自该化合物的公开数据库参考记录。
