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9,9-pinacolato-9-silafluorene

中文名称
——
中文别名
——
英文名称
9,9-pinacolato-9-silafluorene
英文别名
4,4,5,5-Tetramethylspiro[1,3,2-dioxasilolane-2,5'-benzo[b][1]benzosilole];4,4,5,5-tetramethylspiro[1,3,2-dioxasilolane-2,5'-benzo[b][1]benzosilole]
9,9-pinacolato-9-silafluorene化学式
CAS
——
化学式
C18H20O2Si
mdl
——
分子量
296.441
InChiKey
AYSUZNDOMNIVCE-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):
    2.83
  • 重原子数:
    21
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    9,9-pinacolato-9-silafluorene苯基溴化镁四氢呋喃 为溶剂, 反应 1.0h, 以85%的产率得到9-isopropoxy-9-silafluorene
    参考文献:
    名称:
    9,9-二烷氧基-9-硅芴的合成、结构和反应性
    摘要:
    AbstractA series of novel 9,9‐dialkoxy‐9‐silafluorenes were synthesized, and their structures and reactivity were studied. Dehydrogenative alkoxylation of 9,9‐dihydro‐9‐silafluorene with various alcohols in the presence of PdCl2 gave the corresponding dialkoxylated products in good yields. The structures of some of the novel 9,9‐dialkoxy‐9‐silafluorenes were analyzed by X‐ray crystallography. The 9,9‐dialkoxy‐9‐silafluorenes show remarkably high reactivity toward phenylmagnesium bromide to afford substitution products.
    DOI:
    10.1002/hc.21478
  • 作为产物:
    描述:
    2,2'-双溴双苯 在 palladium dichloride 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 6.0h, 生成 9,9-pinacolato-9-silafluorene
    参考文献:
    名称:
    9,9-二烷氧基-9-硅芴的合成、结构和反应性
    摘要:
    AbstractA series of novel 9,9‐dialkoxy‐9‐silafluorenes were synthesized, and their structures and reactivity were studied. Dehydrogenative alkoxylation of 9,9‐dihydro‐9‐silafluorene with various alcohols in the presence of PdCl2 gave the corresponding dialkoxylated products in good yields. The structures of some of the novel 9,9‐dialkoxy‐9‐silafluorenes were analyzed by X‐ray crystallography. The 9,9‐dialkoxy‐9‐silafluorenes show remarkably high reactivity toward phenylmagnesium bromide to afford substitution products.
    DOI:
    10.1002/hc.21478
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文献信息

  • Synthesis, structures, and reactivity of 9,9-dialkoxy-9-silafluorenes
    作者:Ken-ichiro Kanno、Satoshi Hirose、Soichiro Kyushin
    DOI:10.1002/hc.21478
    日期:2018.12
    AbstractA series of novel 9,9‐dialkoxy‐9‐silafluorenes were synthesized, and their structures and reactivity were studied. Dehydrogenative alkoxylation of 9,9‐dihydro‐9‐silafluorene with various alcohols in the presence of PdCl2 gave the corresponding dialkoxylated products in good yields. The structures of some of the novel 9,9‐dialkoxy‐9‐silafluorenes were analyzed by X‐ray crystallography. The 9,9‐dialkoxy‐9‐silafluorenes show remarkably high reactivity toward phenylmagnesium bromide to afford substitution products.
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同类化合物

2,9-二(2-苯乙基)蒽并[2,1,9-DEF:6,5,10-D’E’F’]二异喹啉-1,3,8,10(2H,9H)-四酮 (βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-(+)-5,5'',6,6'',7,7'',8,8''-八氢-3,3''-二叔丁基-1,1''-二-2-萘酚,双钾盐 (S)-盐酸沙丁胺醇 (S)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2-N-Fmoc-氨基甲基吡咯烷盐酸盐 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-7,7-双[(4S)-(苯基)恶唑-2-基)]-2,2,3,3-四氢-1,1-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-3,3''-双([[1,1''-联苯]-4-基)-[1,1''-联萘]-2,2''-二醇 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,5R)-3,3a,8,8a-四氢茚并[1,2-d]-1,2,3-氧杂噻唑-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aS,8aR)-2-(吡啶-2-基)-8,8a-二氢-3aH-茚并[1,2-d]恶唑 (3aS,3''aS,8aR,8''aR)-2,2''-环戊二烯双[3a,8a-二氢-8H-茚并[1,2-d]恶唑] (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3S,3aR)-2-(3-氯-4-氰基苯基)-3-环戊基-3,3a,4,5-四氢-2H-苯并[g]吲唑-7-羧酸 (3R,3’’R,4S,4’’S,11bS,11’’bS)-(+)-4,4’’-二叔丁基-4,4’’,5,5’’-四氢-3,3’’-联-3H-二萘酚[2,1-c:1’’,2’’-e]膦(S)-BINAPINE (3-三苯基甲氨基甲基)吡啶 (3-[(E)-1-氰基-2-乙氧基-2-hydroxyethenyl]-1-氧代-1H-茚-2-甲酰胺) (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,4S)-Fmoc-4-三氟甲基吡咯烷-2-羧酸 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,3R)-3-(叔丁基)-2-(二叔丁基膦基)-4-甲氧基-2,3-二氢苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S,2''S,3S,3''S)-3,3''-二叔丁基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2R,2''R,3R,3''R)-3,3''-二叔丁基-4,4''-二甲氧基-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2-硝基苯基)磷酸三酰胺 (2-氯-6-羟基苯基)硼酸 (2-氟-3-异丙氧基苯基)三氟硼酸钾 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1α,1'R,4β)-4-甲氧基-5''-甲基-6'-[5-(1-丙炔基-1)-3-吡啶基]双螺[环己烷-1,2'-[2H]indene (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1R,1′R,2S,2′S)-2,2′-二叔丁基-2,3,2′,3′-四氢-1H,1′H-(1,1′)二异磷哚