(dichloro)(4-methoxyphenyl)(phenyl)silane

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (dichloro)(4-methoxyphenyl)(phenyl)silane
• 英文别名: Dichloro-(4-methoxyphenyl)-phenylsilane
• 化学式: C₁₃H₁₂Cl₂OSi
• 分子量: 283.229
• InChiKey: RYLSDUHLNUROTK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.73
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (dichloro)(4-methoxyphenyl)(phenyl)silane 在 copper (II)-fluoride 作用下， 以 乙醚 为溶剂， 反应 8.0h， 以47%的产率得到(二氟)(4-甲氧基苯基)(苯基)硅烷
  参考文献：
  名称：

  Highly selective cross-coupling reactions of aryl(halo)silanes with aryl halides: A general and practical route to functionalized biaryls

  摘要：

  The palladium catalyzed cross-coupling reaction of aryl halides with aryl(halo)silanes (halogen= F, Cl) gives good yields of unsymmetrical biaryls and p-terphenyls. The reaction takes place smoothly in N,N-dimethylformamide in the presence of an appropriate palladium catalyst and potassium fluoride. Since this reaction is tolerant of a variety of reactive functional groups, highly functionalized 4,4'-, 3,4'-, 2,4'- and even sterically crowded 2,2'-disubstituted biaryls can be obtained in moderate to high yields. The synthetic utility of the method has been demonstrated by its application to a short synthesis of liquid crystals. Mechanistic aspects of transmetalation of an aryl(fluoro)silicate intermediate with a palladium complex are discussed on the basis of the substituent effects on the rate of the cross-coupling reactions.

  DOI：

  10.1016/s0040-4020(01)85554-x
• 作为产物：
  描述：

  4-溴苯甲醚 、 苯基三氯硅烷 在 碘 、 magnesium 作用下， 以 四氢呋喃 为溶剂， 反应 11.5h， 生成 (dichloro)(4-methoxyphenyl)(phenyl)silane
  参考文献：
  名称：

  Rh催化环化二乙烯基硅烷和烯丙胺合成硅环己酮

  摘要：

  通过[Rh(coe) 2 Cl] 2 /PCy 3催化的二乙烯基硅烷与Jun's烯丙胺的环化，开发了一种有效合成具有多种甲硅烷基取代基的硅环己酮。硅杂环己酮可以用 DDQ 氧化得到相应的硅环己二烯酮，其进一步转化为 2-脱氧链霉胺或外亚烷基硅环己二烯的硅类似物。

  DOI：

  10.1021/acs.orglett.1c04183

文献信息

• Hatanaka Yasuo, Goda Ken-ichi, Okahara Yoshinori, Hiyama Tamejiro, Tetrahedron, 50 (1994) N 28, S 8301-8316
  作者：Hatanaka Yasuo, Goda Ken-ichi, Okahara Yoshinori, Hiyama Tamejiro

  DOI：——

  日期：——
• Synthesis of Silacyclohexanones from Divinylsilanes and Allylamines by a Rh-Catalyzed Cyclization
  作者：Jiawei Guo、Song Liu、Qinjiao Pang、Hongyun Zhang、Lu Gao、Li Chen、Zhenlei Song

  DOI：10.1021/acs.orglett.1c04183

  日期：2022.1.21

  An efficient synthesis of silacyclohexanones bearing a variety of silyl substituents has been developed by a [Rh(coe)2Cl]2/PCy3-catalyzed cyclization of divinylsilanes with Jun’s allylamine. The silacyclohexanones can be oxidized with DDQ to give the corresponding silacyclohexadienones, which are further transformed into silicon analog of 2-deoxystreptamine or exo-alkylidenesilacyclohexadienes.

  通过[Rh(coe) 2 Cl] 2 /PCy 3催化的二乙烯基硅烷与Jun's烯丙胺的环化，开发了一种有效合成具有多种甲硅烷基取代基的硅环己酮。硅杂环己酮可以用 DDQ 氧化得到相应的硅环己二烯酮，其进一步转化为 2-脱氧链霉胺或外亚烷基硅环己二烯的硅类似物。
• Highly selective cross-coupling reactions of aryl(halo)silanes with aryl halides: A general and practical route to functionalized biaryls
  作者：Yasuo Hatanaka、Ken-ichi Goda、Yoshinori Okahara、Tamejiro Hiyama

  DOI：10.1016/s0040-4020(01)85554-x

  日期：1994.1

  The palladium catalyzed cross-coupling reaction of aryl halides with aryl(halo)silanes (halogen= F, Cl) gives good yields of unsymmetrical biaryls and p-terphenyls. The reaction takes place smoothly in N,N-dimethylformamide in the presence of an appropriate palladium catalyst and potassium fluoride. Since this reaction is tolerant of a variety of reactive functional groups, highly functionalized 4,4'-, 3,4'-, 2,4'- and even sterically crowded 2,2'-disubstituted biaryls can be obtained in moderate to high yields. The synthetic utility of the method has been demonstrated by its application to a short synthesis of liquid crystals. Mechanistic aspects of transmetalation of an aryl(fluoro)silicate intermediate with a palladium complex are discussed on the basis of the substituent effects on the rate of the cross-coupling reactions.