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1,1,1-trifluoro-3-difluoromethoxypropane

中文名称
——
中文别名
——
英文名称
1,1,1-trifluoro-3-difluoromethoxypropane
英文别名
3,3,3-Trifluoropropyl difluoromethylether;3-(difluoromethoxy)-1,1,1-trifluoropropane
1,1,1-trifluoro-3-difluoromethoxypropane化学式
CAS
——
化学式
C4H5F5O
mdl
——
分子量
164.075
InChiKey
CBHFRMQTMWUHAI-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):
    2.5
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    氟里昂-223,3,3-三氟-1-丙醇sodium hydroxide 作用下, 以 1,4-二氧六环 为溶剂, 反应 1.0h, 以17%的产率得到1,1,1-trifluoro-3-difluoromethoxypropane
    参考文献:
    名称:
    Reactions of aliphatic fluoro-alcohols with CHClF2 at atmospheric pressure
    摘要:
    The reactions of aliphatic fluoro-alcohols with chlorodifluoromethane (CHCIF2) at atmospheric pressure were examined. In the reaction of CF3CF2CH2OH, the difluoromethylated ether was obtained in moderate yield by using ethers such as 1,4-dioxane, diglyme and THF, or their mixtures with water as a reaction solvent. While acetal and orthoformate were also produced, the selectivity of the difluoromethylated ether could be improved by adding water to the reaction. The effect of water could be explained by the reaction mechanism. (c) 2006 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2005.12.034
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文献信息

  • Reactions of aliphatic fluoro-alcohols with CHClF2 at atmospheric pressure
    作者:Junji Mizukado、Yasuhisa Matsukawa、Heng-dao Quan、Masanori Tamura、Akira Sekiya
    DOI:10.1016/j.jfluchem.2005.12.034
    日期:2006.3
    The reactions of aliphatic fluoro-alcohols with chlorodifluoromethane (CHCIF2) at atmospheric pressure were examined. In the reaction of CF3CF2CH2OH, the difluoromethylated ether was obtained in moderate yield by using ethers such as 1,4-dioxane, diglyme and THF, or their mixtures with water as a reaction solvent. While acetal and orthoformate were also produced, the selectivity of the difluoromethylated ether could be improved by adding water to the reaction. The effect of water could be explained by the reaction mechanism. (c) 2006 Elsevier B.V. All rights reserved.
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