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(E)-1-(1,2-dichlorovinyloxy)-2-methoxybenzene

中文名称
——
中文别名
——
英文名称
(E)-1-(1,2-dichlorovinyloxy)-2-methoxybenzene
英文别名
1-[(E)-1,2-dichloroethenoxy]-2-methoxybenzene
(E)-1-(1,2-dichlorovinyloxy)-2-methoxybenzene化学式
CAS
——
化学式
C9H8Cl2O2
mdl
——
分子量
219.067
InChiKey
UTTGPJWXUAXOGR-TWGQIWQCSA-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):
    3.2
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    三氯乙烯木榴油caesium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 1.5h, 以99%的产率得到(E)-1-(1,2-dichlorovinyloxy)-2-methoxybenzene
    参考文献:
    名称:
    Cs2CO3-Promoted Vinylation of Phenols with Trichloroethylene: Facile Synthesis of (E)-1,2-Dichloro-1-phenoxyethenes
    摘要:
    An efficient method for the synthesis of (E)-1,2-dichloro- 1-phenoxyethenes 2 has been developed. The reaction of phenol derivatives 1 with trichloroethylene at ambient temperature by means of Cs2CO3-DMSO system furnished the corresponding aryl vinyl ethers 2 in excellent yields. On the other hand, the same reaction of phenol derivatives li, 1k and 1p possessing an electron-withdrawing group at the o- or p-position of the hydroxy group required a harsh reaction conditions to heat at 70 degrees C for the synthesis of the desired products 2i, 2k and 2p.
    DOI:
    10.3987/com-18-13953
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文献信息

  • PHOTOCHROMIC AND ELECTROCHROMIC DIARYLCYCLOPENTENE DERIVATIVES AS OPTICAL FILTERS
    申请人:Switch Materials, Inc.
    公开号:EP2760969A1
    公开(公告)日:2014-08-06
  • [EN] PHOTOCHROMIC AND ELECTROCHROMIC DIARYLCYCLOPENTENE DERIVATIVES AS OPTICAL FILTERS<br/>[FR] DÉRIVÉS DE DIARYLCYCLOPENTÈNE PHOTOCHROMES ET ÉLECTROCHROMES COMME FILTRES OPTIQUES
    申请人:SWITCH MATERIALS INC
    公开号:WO2013044371A1
    公开(公告)日:2013-04-04
    A compound according to Formula IA and IB, reversibly convertible under photochromic and electrochromic conditions between a ring-open isomer A and a ring-closed isomer B is provided. For substitutent groups, Z is N, O or S; each R1 is independently selected from the group consisting of H, or halo; each R2 is independently selected from the group consisting of H, halo, a polymer backbone, alkyl or aryl; or, when both R2 together form -CH=CH- and form part of a polymer backbone; each R3 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl; each R4 is aryl; and each R5 is independently selected from the group consisting of H, halo, alkyl, alkoxy, thioalkyl or aryl.
  • Cs2CO3-Promoted Vinylation of Phenols with Trichloroethylene: Facile Synthesis of (E)-1,2-Dichloro-1-phenoxyethenes
    作者:Kazunori Takahashi、Naho Mamiya、Kei Fukushima、Masayoshi Tsubuki、Toshio Honda
    DOI:10.3987/com-18-13953
    日期:——
    An efficient method for the synthesis of (E)-1,2-dichloro- 1-phenoxyethenes 2 has been developed. The reaction of phenol derivatives 1 with trichloroethylene at ambient temperature by means of Cs2CO3-DMSO system furnished the corresponding aryl vinyl ethers 2 in excellent yields. On the other hand, the same reaction of phenol derivatives li, 1k and 1p possessing an electron-withdrawing group at the o- or p-position of the hydroxy group required a harsh reaction conditions to heat at 70 degrees C for the synthesis of the desired products 2i, 2k and 2p.
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