反应 #4127773
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-dd9798038e6e477d838f388435326290暂无可渲染的结构数据
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顺-4-甲胺基环己醇(CAS 22348-44-3)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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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-dd9798038e6e477d838f388435326290反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4b8fa99d7ebd4643ad16360ff0c8923a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f88aa8030b0f4a1b990bc355404d8f45反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2acf0bd861114d3a866b18c547518e32反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0353c4dbeee049fc8c3d52e30a20947c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following procedures similar to those described in Example 260 there was obtained from 64.6 g. of 4-methylaminocyclohexanol, on reaction with 87.2 g. of 4-fluorobenzoyl chloride, 100.6 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanol, m.p. 120°-130° C., 25.1 g. of which were oxidized to give 22.3 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanone, m.p. 132°-136° C. was obtained from 64.6 g to give 22.3 g
来源 ID: ord-3cabd50f6d864779bba5b0562a0691d4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following procedures similar to those described in Example 260 there was obtained from 64.6 g. of 4-methylaminocyclohexanol, on reaction with 87.2 g. of 4-fluorobenzoyl chloride, 100.6 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanol, m.p. 120°-130° C., 25.1 g. of which were oxidized to give 22.3 g. of 4-(N-methyl-4 -fluorobenzamido)-cyclohexanone, m.p. 132°-136° C. was obtained from 64.6 g to give 22.3 g
来源 ID: ord-cbc90800ea664cefaf90a5ffd04606cd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following procedures similar to those described in Example 260 there was obtained from 64.6 g. of 4-methylaminocyclohexanol, on reaction with 87.2 g. of 4-fluorobenzoyl chloride, 100.6 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanol, m.p. 120°-130° C., 25.1 g. of which were oxidized to give 22.3 g. of 4-(N-methyl-4 -fluorobenzamido)-cyclohexanone, m.p. 132°-136° C. was obtained from 64.6 g to give 22.3 g
来源 ID: ord-cbc90800ea664cefaf90a5ffd04606cd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following procedures similar to those described in Example 260 there was obtained from 64.6 g. of 4-methylaminocyclohexanol, on reaction with 87.2 g. of 4-fluorobenzoyl chloride, 100.6 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanol, m.p. 120°-130° C., 25.1 g. of which were oxidized to give 22.3 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanone, m.p. 132°-136° C. was obtained from 64.6 g to give 22.3 g
来源 ID: ord-3cabd50f6d864779bba5b0562a0691d4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following procedures similar to those described in Example 260 there was obtained from 64.6 g. of 4-methylaminocyclohexanol, on reaction with 87.2 g. of 4-fluorobenzoyl chloride, 100.6 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanol, m.p. 120°-130° C., 25.1 g. of which were oxidized to give 22.3 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanone, m.p. 132°-136° C. was obtained from 64.6 g to give 22.3 g
来源 ID: ord-3cabd50f6d864779bba5b0562a0691d4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following procedures similar to those described in Example 260 there was obtained from 64.6 g. of 4-methylaminocyclohexanol, on reaction with 87.2 g. of 4-fluorobenzoyl chloride, 100.6 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanol, m.p. 120°-130° C., 25.1 g. of which were oxidized to give 22.3 g. of 4-(N-methyl-4-fluorobenzamido)-cyclohexanone, m.p. 132°-136° C. was obtained from 64.6 g to give 22.3 g
来源 ID: ord-c57a1b9fefa64cf0a6532bc89c724ec8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-dd9798038e6e477d838f388435326290PubChem References
以下资料来自该化合物的公开数据库参考记录。
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