2,2-dimethyl-2H-benzo[e][1,2]oxasiline | 62037-32-5

• 分子结构分类: 有机化合物 - 苯类化合物
• 英文名称: 2,2-dimethyl-2H-benzo[e][1,2]oxasiline
• 英文别名: 2,2-dimethyl-2H-benzo[e][1,2]oxasiline；2,2-Dimethylsiloxaronaphthalin；2H-1,2-Benzoxasilin, 2,2-dimethyl-；2,2-dimethyl-1,2-benzoxasiline
• CAS: 62037-32-5
• 化学式: C₁₀H₁₂OSi
• 分子量: 176.29
• InChiKey: BMEVOQLLBNXJNX-UHFFFAOYSA-N

物化性质

• 沸点：
  196.6±33.0 °C(Predicted)
• 密度：
  1.02±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.84
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  (2-溴苯氧基)二甲基(乙烯基)硅烷 在 bis(η3-allyl-μ-chloropalladium(II)) 、 lithium tert-butoxide 、 2-二环己基磷-2,4,6-三异丙基联苯 作用下， 以 甲苯 为溶剂， 反应 12.0h， 以51%的产率得到2,2-dimethyl-2H-benzo[e][1,2]oxasiline
  参考文献：
  名称：

  Construction of Benzosiloles, Six- and Eight-Membered Silacyclic Skeletons, via a Pd-Catalyzed Intramolecular Mizoroki–Heck Reaction of Vinylsilanes

  摘要：

  A variety of silacycles including benzosiloles, six- and eight-membered silacyclic skeletons, were efficiently synthesized via a Pd-catalyzed intramolecular Mizoroki-Heck reaction of vinylsilanes.

  DOI：

  10.1021/ol302040j

文献信息

• Photochemically Removable Silyl Protecting Groups
  作者：Michael C. Pirrung、Lara Fallon、Jin Zhu、Yong Rok Lee

  DOI：10.1021/ja002370t

  日期：2001.4.1

  Several o-phenol-containing alkoxyvinylsilanes were prepared and their photochemistry was investigated. These materials were prepared via hydrosilylation of the corresponding o-acetoxy arylacetylenes. Two major classes of photochemical processes were identified in these reactants: trans --> cia isomerization, leading to an intramolecular nucleophilic substitution process at silicon, and 1,5-silyl shift, leading to an unsymmetrical dialkoxysilane. The major outcome of this work is a novel class of photochemically removable protecting groups. Two alkyl substitutions on silicon, the dimethyl and diisopropyl, were examined. The latter is more stable and is preferred for protecting groups that must tolerate multiple steps or reagents. Protection of alcohols is generally performed starting with the arylethynyl acetate, which can be subjected to hydrosilylation, alcohol substitution, and acetate deprotection without isolation of intermediates. Two groups were studied in detail, the phenol and 2 naphthol Vinyl silane derivatives. A variety of primary and secondary alcohols were protected with these reagents. These groups can be deprotected cleanly and in high yield by irradiation from 250 to 350 nm.
• Photochemically-removable silyl protecting groups
  作者：Michael C. Pirrung、Yong Rok Lee

  DOI：10.1021/jo00077a010

  日期：1993.12

  (Hydroxystyryl)dimethylsilyl (HSDMS) and (hydroxystyryl)diisopropylsilyl (HSDIS) reagents have been developed that readily protect primary and secondary alcohols and can be removed on irradiation with short wavelength light in polar solvent.
• Construction of Benzosiloles, Six- and Eight-Membered Silacyclic Skeletons, via a Pd-Catalyzed Intramolecular Mizoroki–Heck Reaction of Vinylsilanes
  作者：Kunbing Ouyang、Yun Liang、Zhenfeng Xi

  DOI：10.1021/ol302040j

  日期：2012.9.7

  A variety of silacycles including benzosiloles, six- and eight-membered silacyclic skeletons, were efficiently synthesized via a Pd-catalyzed intramolecular Mizoroki-Heck reaction of vinylsilanes.