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2-ethoxycarbonylmethyl-1-methyl-1,2-dihydroquinoline | 151323-85-2

中文名称
——
中文别名
——
英文名称
2-ethoxycarbonylmethyl-1-methyl-1,2-dihydroquinoline
英文别名
2-ethoxycarbonylmethyl-1,2-dihydro-1-methylquinoline;ethyl 2-(1-methyl-2H-quinolin-2-yl)acetate
2-ethoxycarbonylmethyl-1-methyl-1,2-dihydroquinoline化学式
CAS
151323-85-2
化学式
C14H17NO2
mdl
——
分子量
231.294
InChiKey
ODUQUVANNORSTE-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    337.0±35.0 °C(Predicted)
  • 密度:
    1.077±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-ethoxycarbonylmethyl-1-methyl-1,2-dihydroquinoline氘代氯仿 为溶剂, 反应 1680.0h, 以98%的产率得到(E)-2-ethoxycarbonylmethylidene-1,2,3,4-tetrahydro-1-methylquinoline
    参考文献:
    名称:
    Silicon-Assisted Ethoxycarbonylmethylation ofN-Methylquinolinium and Isoquinolinium Iodides
    摘要:
    A new regioselective route to 2-ethoxycarbonylmethyl- 1,2-dihydro-N-methylquinolines and 1-ethoxycarbonylmethyl-1,2-dihydro-N-methylisoquinolines is described starting from methylquinolinium or -isoquinolinium iodides and commercially available ethyltrimethylsilyl acetate (ETSA). The methylene carbanion was generated by fluorodesilylation using caesium fluoride. On exposure to air, the ethoxycarbonylmethyl adducts were oxidised, leading to the corresponding alkylidene derivatives 4 and 5, whereas 2a in solution led slowly to its regioisomer 6a.
    DOI:
    10.1002/1099-0690(200008)2000:16<2915::aid-ejoc2915>3.0.co;2-b
  • 作为产物:
    描述:
    (三甲基硅基)乙酸乙酯N-methylquinolinium iodide 在 cesium fluoride 作用下, 以 乙腈 为溶剂, 反应 2.0h, 以86%的产率得到2-ethoxycarbonylmethyl-1-methyl-1,2-dihydroquinoline
    参考文献:
    名称:
    乙氧基羰基甲基和氰基甲基的区域选择性引入喹啉和异喹啉
    摘要:
    提出了从甲基喹啉鎓或-异喹啉鎓碘化物和市售三甲基甲硅烷基试剂开始的乙氧基羰基甲基-和氰基甲基-1,2-二氢-N-甲基喹啉和-异喹啉的区域选择性新路线。
    DOI:
    10.1039/a802694g
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文献信息

  • Regioselective Introduction of Ethoxycarbonylmethyl and Cyanomethyl Groups into Quinoline and Isoquinoline
    作者:Micheline Grignon-Dubois、Faı¨za Diaba
    DOI:10.1039/a802694g
    日期:——
    A new regioselective route to ethoxycarbonylmethyl- and cyanomethyl-1,2-dihydro-N-methyl-quinolines and -isoquinolines starting from methyl-quinolinium or -isoquinolinium iodides and commercially available trimethylsilyl reagents is presented.
    提出了从甲基喹啉鎓或-异喹啉鎓碘化物和市售三甲基甲硅烷基试剂开始的乙氧基羰基甲基-和氰基甲基-1,2-二氢-N-甲基喹啉和-异喹啉的区域选择性新路线。
  • Fine Control of Regioselectivity in the Reduction of NAD<sup>+</sup>Analogues by Ketene Silyl Acetals
    作者:Shunichi Fukuzumi、Morifumi Fujita、Souta Noura、Junzo Otera
    DOI:10.1246/cl.1993.1025
    日期:1993.6
    Various NAD+ analogues are reduced regioselectively by ketene silyl acetals to afford the corresponding 2-, 6-, or 4-alkylated NADH analogues. The regioselectivity of the 1,2- (or 1,6-) vs. 1,4-reduction is finely controlled by the β-methyl-substitution of ketene silyl acetals, the position of methyl-substitution of NAD+ analogues, and the addition of Et4NCl or Bu4NF.
    各种 NAD+ 类似物通过乙缩酮硅烷进行区域选择性还原,从而得到相应的 2-、6- 或 4-烷基化 NADH 类似物。1,2-(或 1,6-)与 1,4-还原的区域选择性受烯甲硅基乙醛的 β-甲基取代、NAD+ 类似物的甲基取代位置以及 Et4NCl 或 Bu4NF 的添加等因素的严格控制。
  • Silicon-Assisted Ethoxycarbonylmethylation ofN-Methylquinolinium and Isoquinolinium Iodides
    作者:Faïza Diaba、Cyril Le Houerou、Micheline Grignon-Dubois、Bernadette Rezzonico、Pierre Gerval
    DOI:10.1002/1099-0690(200008)2000:16<2915::aid-ejoc2915>3.0.co;2-b
    日期:2000.8
    A new regioselective route to 2-ethoxycarbonylmethyl- 1,2-dihydro-N-methylquinolines and 1-ethoxycarbonylmethyl-1,2-dihydro-N-methylisoquinolines is described starting from methylquinolinium or -isoquinolinium iodides and commercially available ethyltrimethylsilyl acetate (ETSA). The methylene carbanion was generated by fluorodesilylation using caesium fluoride. On exposure to air, the ethoxycarbonylmethyl adducts were oxidised, leading to the corresponding alkylidene derivatives 4 and 5, whereas 2a in solution led slowly to its regioisomer 6a.
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