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4,4-difluoro-3,3-dimethyl-1-butene

中文名称
——
中文别名
——
英文名称
4,4-difluoro-3,3-dimethyl-1-butene
英文别名
4,4-Difluoro-3,3-dimethylbut-1-ene
4,4-difluoro-3,3-dimethyl-1-butene化学式
CAS
——
化学式
C6H10F2
mdl
——
分子量
120.142
InChiKey
AORHKLZZILVKFT-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):
    3.1
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    3-氯-3-甲基-1-丁烯 、 difluoromethyl copper 以 N,N-二甲基甲酰胺 为溶剂, 反应 5.0h, 以76%的产率得到4,4-difluoro-3,3-dimethyl-1-butene
    参考文献:
    名称:
    The preparation of HCF2CdX and HCF2ZnX via direct insertion into the carbon halogen bond of CF2HY (Y=Br, I)
    摘要:
    The difluoromethylcadmium and zinc reagents have been prepared in DMF via direct insertion of Cd-0 into the carbon halogen bond of CF2HY (Y = Br, I). These reagents are stable at 65-75 degrees C and exhibit prolonged stability and activity at room temperature. Metathesis of the difluoromethylcadmium reagents with Cu(I)X (X = Br, Cl) at -55 degrees C rapidly produces difluoromethylcopper. The copper reagent is significantly less stable than the cadmium or zinc reagent and rapidly decomposes at room temperature. The difluoromethylcadmium and copper reagents exhibit good reactivity with allylic halides, propargylic derivatives and 1-iodoalkynes to provide good yields of the corresponding difluoromethylalkenes, difluoromethylallenes and difluoromethyl-2-alkynes. Alkylation is successful only with reactive alkyl halides. Generally, the difluoromethylcopper reagent is more reactive than the difluoromethylcadmium reagent and generally exhibits higher regioselectivity in reactions that can occur by either alpha- or -gamma-attack. (C) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jfluchem.2007.05.015
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文献信息

  • Ink composition, inkjetrecording method, printed material, method for producing planographic printing plate, and planographic printing plate
    申请人:FUJIFILM Corporation
    公开号:EP1964894A2
    公开(公告)日:2008-09-03
    There are provided an ink composition including at least an initiator, a polymerizable monomer and a polymer comprising a fluorine containing group and a polymerizable group; an inkjet recording method using the ink composition; a printed material recorded by the inkjet recording method; a method of producing a planographic printing plate using the ink composition; and a planographic printing plate obtained by the method of producing a planographic printing plate.
    提供了一种墨水组合物,其中至少包括一种引发剂、一种可聚合单体和一种包含含氟基团和可聚合基团的聚合物;一种使用该墨水组合物的喷墨记录方法;一种通过该喷墨记录方法记录的印刷材料;一种使用该墨水组合物制作平版印刷板的方法;以及一种通过该制作平版印刷板的方法获得的平版印刷板。
  • Ink composition, inkjet recording method and process for producing molded printed material
    申请人:Fujifilm Corporation
    公开号:EP2371910A1
    公开(公告)日:2011-10-05
    An ink composition is provided that includes (Component a) an open-chain and/or cyclic ether bond-containing monofunctional (meth)acrylate, (Component b) one or more monofunctional ethylenically unsaturated compounds selected from the group consisting of a polycyclic aliphatic group-containing monofunctional (meth)acrylate and N-vinyl-2-caprolactam, (Component c) a polymerization initiator, (Component e) a polyfunctional (meth)acrylate at no greater than 10 wt % relative to the ink composition, and (Component f) a fluorine-substituted hydrocarbon group- or siloxane structure-containing polymer, the ratio by weight of (Component a)/(Component b) being 0.7 to 1.9. There are also provided an inkjet recording method that includes (a1) an image formation step of forming an image above a recording medium by discharging the ink composition by an inkjet method and (b1) a curing step of curing the ink composition by irradiating the obtained image with actinic radiation to thus obtain a cured image above the recording medium, and a process for producing a molded printed material that includes (a2) an image formation step of forming an image above a recording medium by discharging the ink composition by an inkjet method, (b2) a curing step of curing the ink composition by irradiating the obtained image with actinic radiation to thus obtain a printed material having a cured image above the recording medium, and (c2) a molding step of molding the printed material.
    提供了一种油墨组合物,其中包括(组分 a)含开链和/或环醚键的单官能团(甲基)丙烯酸酯,(组分 b)一种或多种单官能团乙烯基不饱和化合物,这些化合物选自由含多环脂肪族单官能团(甲基)丙烯酸酯和 N-乙烯基-2-己内酰胺组成的组、(组分 c)聚合引发剂,(组分 e)多官能度(甲基)丙烯酸酯,相对于油墨组合物不大于 10 wt %,和(组分 f)含氟取代烃基或硅氧烷结构的聚合物,(组分 a)/(组分 b)的重量比为 0.7至1.9。还提供了一种喷墨记录方法,该方法包括:(a1) 图像形成步骤,即通过喷墨方法排放墨水组合物,在记录介质上方形成图像;(b1) 固化步骤,即通过用阳极辐射照射获得的图像,使墨水组合物固化,从而在记录介质上方获得固化图像、以及一种用于生产模制印刷材料的工艺,该工艺包括:(a2) 通过喷墨方法在记录介质上方排放墨水组合物以形成图像的图像形成步骤;(b2) 通过用阳极辐射照射获得的图像以固化墨水组合物从而获得在记录介质上方具有固化图像的印刷材料的固化步骤;(c2) 模制印刷材料的模制步骤。
  • The preparation and allylation of difluoromethylcadmium
    作者:Greg A. Hartgraves、Donald J. Burton
    DOI:10.1016/s0022-1139(00)81613-9
    日期:1988.6
  • The preparation of HCF2CdX and HCF2ZnX via direct insertion into the carbon halogen bond of CF2HY (Y=Br, I)
    作者:Donald J. Burton、Greg A. Hartgraves
    DOI:10.1016/j.jfluchem.2007.05.015
    日期:2007.10
    The difluoromethylcadmium and zinc reagents have been prepared in DMF via direct insertion of Cd-0 into the carbon halogen bond of CF2HY (Y = Br, I). These reagents are stable at 65-75 degrees C and exhibit prolonged stability and activity at room temperature. Metathesis of the difluoromethylcadmium reagents with Cu(I)X (X = Br, Cl) at -55 degrees C rapidly produces difluoromethylcopper. The copper reagent is significantly less stable than the cadmium or zinc reagent and rapidly decomposes at room temperature. The difluoromethylcadmium and copper reagents exhibit good reactivity with allylic halides, propargylic derivatives and 1-iodoalkynes to provide good yields of the corresponding difluoromethylalkenes, difluoromethylallenes and difluoromethyl-2-alkynes. Alkylation is successful only with reactive alkyl halides. Generally, the difluoromethylcopper reagent is more reactive than the difluoromethylcadmium reagent and generally exhibits higher regioselectivity in reactions that can occur by either alpha- or -gamma-attack. (C) 2007 Elsevier B.V. All rights reserved.
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