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1-(difluoromethoxy)hexadecane | 1333375-77-1

中文名称
——
中文别名
——
英文名称
1-(difluoromethoxy)hexadecane
英文别名
——
1-(difluoromethoxy)hexadecane化学式
CAS
1333375-77-1
化学式
C17H34F2O
mdl
——
分子量
292.453
InChiKey
SIMLLQPQYMHODQ-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):
    6.71
  • 重原子数:
    20.0
  • 可旋转键数:
    16.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.23
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

反应信息

  • 作为产物:
    描述:
    1-十六烷醇 、 N,N-dimethyl-S-difluoromethyl-S-phenylsulfoximinium tetrafluoroborate 以 二氯甲烷 为溶剂, 反应 1.0h, 以25%的产率得到1-(difluoromethoxy)hexadecane
    参考文献:
    名称:
    N,N-Dimethyl-S-difluoromethyl-S-phenylsulfoximinium tetrafluoroborate: A versatile electrophilic difluoromethylating reagent
    摘要:
    Over the past decade, sulfur-based fluoromethyl containing compounds have been exhaustively investigated as versatile fluoroalkylating reagents by our research laboratory as well as many others. Lately, we have designed a novel electrophilic difluoromethylating protocol employing in situ prepared N,N-dimethyl-S-difluoromethyl-S-phenylsulfoximinium salt. The present reagent provides excellent reactivity toward a broad spectrum of nucleophilic species (N-, P-, S-, and O-nucleophiles) to yield the corresponding difluoromethylated products with high efficacy under mild conditions. Additional studies have been performed to elucidate the mechanistic fundamentals of the reactions. (C) 2011 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2011.04.023
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文献信息

  • Difluoromethylation of alcohols with TMSCF2Br in water: A new insight into the generation and reactions of difluorocarbene in a two-phase system
    作者:Rongyi Zhang、Chuanfa Ni、Qiqiang Xie、Jinbo Hu
    DOI:10.1016/j.tet.2020.131676
    日期:2020.12
    ved reactions can be performed in the presence of water, the reaction of difluorocarbene using water as the only reaction medium is rare. By using TMSCF2Br as a unique difluorocarbene reagent and KHF2 as a mild activator, the difluoromethylation of liquid alcohols in water is described. This research not only develops an environmentally benign process for the synthesis of difluoromethyl ethers, but
    尽管可以在的存在下进行许多涉及二氟卡宾的反应,但是使用作为唯一反应介质的二氟卡宾的反应很少。通过使用TMSCF 2 Br作为独特的二氟卡宾试剂和KHF 2作为温和的活化剂,描述了液体醇在中的二甲基化。这项研究不仅为二甲基醚的合成开发了一种环境友好的方法,而且为油两相系统中二氟卡宾的生成和反应提供了新的见识。
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