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N-(3-chloropropanoyl)-3,4-dihydro-4-methylspiro[quinoline-2,1'-cyclohexane] | 487011-10-9

中文名称
——
中文别名
——
英文名称
N-(3-chloropropanoyl)-3,4-dihydro-4-methylspiro[quinoline-2,1'-cyclohexane]
英文别名
3-Chloro-1-(4-methylspiro[3,4-dihydroquinoline-2,1'-cyclohexane]-1-yl)propan-1-one
N-(3-chloropropanoyl)-3,4-dihydro-4-methylspiro[quinoline-2,1'-cyclohexane]化学式
CAS
487011-10-9
化学式
C18H24ClNO
mdl
——
分子量
305.848
InChiKey
BVBVXARGYQLJQC-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    N-(3-chloropropanoyl)-3,4-dihydro-4-methylspiro[quinoline-2,1'-cyclohexane] 在 lithium aluminium tetrahydride 、 三氯化铝 作用下, 以 乙醚正庚烷 为溶剂, 反应 1.5h, 生成 7-methyl-1,2,6,7-tetrahydrospiro[pyrido-(3,2,1-ij)quinoline-5,1'-cyclohexane]
    参考文献:
    名称:
    Studies directed to the synthesis of new C-5 spiroannulated julolidines
    摘要:
    Two series of new 7,9-disubstituted spirojulolidines 8a-d and 10a-e were synthesized by acid catalyzed intramolecular cyclization of N-(3-chloropropanoyl) spirodihydroquinolines 5a-d and N-carbethoxymethyl spirodihydroquinolines 7a-e using AlCl3 and PPA, respectively. The spectroscopic analyses of intermediate compounds and the final spirojulolidines were discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)01095-5
  • 作为产物:
    描述:
    1,2,3,4-tetrahydro-4-methylspiro3-氯丙酰氯sodium carbonate 作用下, 以 为溶剂, 以34%的产率得到N-(3-chloropropanoyl)-3,4-dihydro-4-methylspiro[quinoline-2,1'-cyclohexane]
    参考文献:
    名称:
    Studies directed to the synthesis of new C-5 spiroannulated julolidines
    摘要:
    Two series of new 7,9-disubstituted spirojulolidines 8a-d and 10a-e were synthesized by acid catalyzed intramolecular cyclization of N-(3-chloropropanoyl) spirodihydroquinolines 5a-d and N-carbethoxymethyl spirodihydroquinolines 7a-e using AlCl3 and PPA, respectively. The spectroscopic analyses of intermediate compounds and the final spirojulolidines were discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)01095-5
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