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1,3-bis(2',2',4',4',6',6'-hexamethylcyclotrisilazanyl)-5-fluoro-2,4,6-trimethylborazine | 477338-46-8

中文名称
——
中文别名
——
英文名称
1,3-bis(2',2',4',4',6',6'-hexamethylcyclotrisilazanyl)-5-fluoro-2,4,6-trimethylborazine
英文别名
1,3-Bis(2',2',4',4',6',6'-hexamethylcyclotrisilazanyl)-5-fluor-2,4,6-trimethylborazin;1-[4-Fluoro-6-(2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatrisilinan-1-yl)-1,3,5-trimethyl-1,3,5,2,4,6-triazatriborinan-2-yl]-2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatrisilinane;1-[4-fluoro-6-(2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatrisilinan-1-yl)-1,3,5-trimethyl-1,3,5,2,4,6-triazatriborinan-2-yl]-2,2,4,4,6,6-hexamethyl-1,3,5,2,4,6-triazatrisilinane
1,3-bis(2',2',4',4',6',6'-hexamethylcyclotrisilazanyl)-5-fluoro-2,4,6-trimethylborazine化学式
CAS
477338-46-8
化学式
C15H49B3FN9Si6
mdl
——
分子量
575.559
InChiKey
MGADQSJWSJNXML-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):
    0.92
  • 重原子数:
    34
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    64.3
  • 氢给体数:
    4
  • 氢受体数:
    10

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    六甲基环三硅氮烷1,3-bis(2',2',4',4',6',6'-hexamethylcyclotrisilazanyl)-5-fluoro-2,4,6-trimethylborazine 在 n-BuLi 作用下, 以 petroleum ether 为溶剂, 以48%的产率得到1,3,5-tris(2',2',4',4',6',6'-hexamethylcyclotrisilazanyl)-2,4,6-trimethylborazine
    参考文献:
    名称:
    Kopplung von Cyclosilazanen mit Aminofluorboranen und Borazinen
    摘要:
    1-Fluorodimethylsilyl-2,2,4,4,6,6-hexamethylcyclotrisilazane reacts with n-BuLi to give the 1-fluorodimethylsilyl-3-lithi- um-2,2,4,4,6,6-hexamethylcyclotrisilazane (1). Starting with F2B-N(CHMe2)(2) and 1 1-diisopropylamino-fluoroboryl-3-fluorodimethylsilyl- and 1,3-bis(diisopropylamino-fluoroboryl)-5-fluorodimethylsilyl-2,2,4,4,6,6-hexamethylcyclotrisilazanes 2 und 3 are formed. 1,3-Bis- and 1,3,5-tris(diisopropylamino-fluoroboryl)2,2,4,4,6,6 -hexamethylcyclotrisilazanes 4 and 5 are the products from F2BN(CHMe2)2 and di- or trilithiated (Me2Si-NH)(3). The dilithium salt of the eight-membered ring (Me2Si-NH)4 reacts with F2B-NR,R'(6: R,R' = CHMe2,7: R = Me, R' = 2,6-C6H3 (CHMe2)(2)) with retention of the ring size to give 1,5-bis(amino-fluoroboryl)-2,2,4,4,6,6,8,8-octamethylcyclotetrasilazanes 6 and 7. Coupling of cyclosilazanes and borazines occurs in the reaction of lithiated cyclotrisilazane and (FB-NR)(3) in a molar ratio 1:1 (8, 9), 2:1 (11, 12), 3:1 (13) and 1:3 (14); Me2Si(NH-SiMe2)(2)N-B(NR-BF)(2)NR (8, 9); [Me2Si(NH-SiMe2)(2)N](2)(BNR)(2)BFNR (11, 12); [Me2Si(NH-SiMe2)(2)N](3)(BNR)(3) (13); (Me2Si-N)(3) (B(NR-BF)(2)NR)(3) (14); (R = Me: 8, 11, 13); (R = Et: 9, 12, 14); 8 reacts with n-BuLi under substitution of the fluorine by n-C4H9 (10). The isomerization of the cyclotri- to the cyclodisilazane in the reaction of the dilithiated (Si-N)(3) ring with 2 (Me3CN-BF)(3) has kinetical reasons. Me3CN(BF-NCMe3)(2)B-NHSiMe2-(N-SiMe2)(2)- B(CMe3N-BF)(2)NCMe3 (15) is formed. Mono- and dilithiated (Me2Si-NH)(4) reacts with (FB-NEt)(3) in a molar ratio 1:1 and 1:2 to give the exptected mono- and disubstituted cyclotetrasilazanes, the isomeric cyclodisilazane, [Me3CN(BF-NCMe3)(2)B-NHSiMe2-N-SiMe2](2) (18) is obtained in the reaction with (Me3CN-BF)(3) in a molar ratio 1:2. Lithium-bis(trimethylsilyl)amide substitutes successively at the (FB-NEt)(3) one or two fluorine atoms. EtN(BF-NEt)(2)B-N(SiMe3)(2) (19) and FB(NEt-B)(2)[N(SiMe3)(2)](2)NEt (20) are formed. 20 reacts with (Me3Si)(2)NH to give Me3SiF and bis(3,5-bis(bis(trimethylsilyl)amino-2,4,6-triethyl)borazinyl)amine (21); [EtN(B-N(SiMe3)(2)NEt)(2)B](2)NH. The crystal structures of 1, 3, 6, 12 - 15, 18 and 21 are reported.
    DOI:
    10.1002/1521-3749(200209)628:9/10<2071::aid-zaac2071>3.0.co;2-k
  • 作为产物:
    描述:
    参考文献:
    名称:
    Kopplung von Cyclosilazanen mit Aminofluorboranen und Borazinen
    摘要:
    1-Fluorodimethylsilyl-2,2,4,4,6,6-hexamethylcyclotrisilazane reacts with n-BuLi to give the 1-fluorodimethylsilyl-3-lithi- um-2,2,4,4,6,6-hexamethylcyclotrisilazane (1). Starting with F2B-N(CHMe2)(2) and 1 1-diisopropylamino-fluoroboryl-3-fluorodimethylsilyl- and 1,3-bis(diisopropylamino-fluoroboryl)-5-fluorodimethylsilyl-2,2,4,4,6,6-hexamethylcyclotrisilazanes 2 und 3 are formed. 1,3-Bis- and 1,3,5-tris(diisopropylamino-fluoroboryl)2,2,4,4,6,6 -hexamethylcyclotrisilazanes 4 and 5 are the products from F2BN(CHMe2)2 and di- or trilithiated (Me2Si-NH)(3). The dilithium salt of the eight-membered ring (Me2Si-NH)4 reacts with F2B-NR,R'(6: R,R' = CHMe2,7: R = Me, R' = 2,6-C6H3 (CHMe2)(2)) with retention of the ring size to give 1,5-bis(amino-fluoroboryl)-2,2,4,4,6,6,8,8-octamethylcyclotetrasilazanes 6 and 7. Coupling of cyclosilazanes and borazines occurs in the reaction of lithiated cyclotrisilazane and (FB-NR)(3) in a molar ratio 1:1 (8, 9), 2:1 (11, 12), 3:1 (13) and 1:3 (14); Me2Si(NH-SiMe2)(2)N-B(NR-BF)(2)NR (8, 9); [Me2Si(NH-SiMe2)(2)N](2)(BNR)(2)BFNR (11, 12); [Me2Si(NH-SiMe2)(2)N](3)(BNR)(3) (13); (Me2Si-N)(3) (B(NR-BF)(2)NR)(3) (14); (R = Me: 8, 11, 13); (R = Et: 9, 12, 14); 8 reacts with n-BuLi under substitution of the fluorine by n-C4H9 (10). The isomerization of the cyclotri- to the cyclodisilazane in the reaction of the dilithiated (Si-N)(3) ring with 2 (Me3CN-BF)(3) has kinetical reasons. Me3CN(BF-NCMe3)(2)B-NHSiMe2-(N-SiMe2)(2)- B(CMe3N-BF)(2)NCMe3 (15) is formed. Mono- and dilithiated (Me2Si-NH)(4) reacts with (FB-NEt)(3) in a molar ratio 1:1 and 1:2 to give the exptected mono- and disubstituted cyclotetrasilazanes, the isomeric cyclodisilazane, [Me3CN(BF-NCMe3)(2)B-NHSiMe2-N-SiMe2](2) (18) is obtained in the reaction with (Me3CN-BF)(3) in a molar ratio 1:2. Lithium-bis(trimethylsilyl)amide substitutes successively at the (FB-NEt)(3) one or two fluorine atoms. EtN(BF-NEt)(2)B-N(SiMe3)(2) (19) and FB(NEt-B)(2)[N(SiMe3)(2)](2)NEt (20) are formed. 20 reacts with (Me3Si)(2)NH to give Me3SiF and bis(3,5-bis(bis(trimethylsilyl)amino-2,4,6-triethyl)borazinyl)amine (21); [EtN(B-N(SiMe3)(2)NEt)(2)B](2)NH. The crystal structures of 1, 3, 6, 12 - 15, 18 and 21 are reported.
    DOI:
    10.1002/1521-3749(200209)628:9/10<2071::aid-zaac2071>3.0.co;2-k
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文献信息

  • Helmold, Nina; Jaschke, Bettina; Klingebiel, Uwe, Phosphorus, Sulfur and Silicon and the Related Elements, 2001, vol. 168-169, p. 245 - 248
    作者:Helmold, Nina、Jaschke, Bettina、Klingebiel, Uwe
    DOI:——
    日期:——
  • Kopplung von Cyclosilazanen mit Aminofluorboranen und Borazinen
    作者:Bettina Jaschke、Nina Helmold、Ilka Müller、Thomas Pape、Mathias Noltemeyer、Regine Herbst-Irmer、Uwe Klingebiel
    DOI:10.1002/1521-3749(200209)628:9/10<2071::aid-zaac2071>3.0.co;2-k
    日期:2002.9
    1-Fluorodimethylsilyl-2,2,4,4,6,6-hexamethylcyclotrisilazane reacts with n-BuLi to give the 1-fluorodimethylsilyl-3-lithi- um-2,2,4,4,6,6-hexamethylcyclotrisilazane (1). Starting with F2B-N(CHMe2)(2) and 1 1-diisopropylamino-fluoroboryl-3-fluorodimethylsilyl- and 1,3-bis(diisopropylamino-fluoroboryl)-5-fluorodimethylsilyl-2,2,4,4,6,6-hexamethylcyclotrisilazanes 2 und 3 are formed. 1,3-Bis- and 1,3,5-tris(diisopropylamino-fluoroboryl)2,2,4,4,6,6 -hexamethylcyclotrisilazanes 4 and 5 are the products from F2BN(CHMe2)2 and di- or trilithiated (Me2Si-NH)(3). The dilithium salt of the eight-membered ring (Me2Si-NH)4 reacts with F2B-NR,R'(6: R,R' = CHMe2,7: R = Me, R' = 2,6-C6H3 (CHMe2)(2)) with retention of the ring size to give 1,5-bis(amino-fluoroboryl)-2,2,4,4,6,6,8,8-octamethylcyclotetrasilazanes 6 and 7. Coupling of cyclosilazanes and borazines occurs in the reaction of lithiated cyclotrisilazane and (FB-NR)(3) in a molar ratio 1:1 (8, 9), 2:1 (11, 12), 3:1 (13) and 1:3 (14); Me2Si(NH-SiMe2)(2)N-B(NR-BF)(2)NR (8, 9); [Me2Si(NH-SiMe2)(2)N](2)(BNR)(2)BFNR (11, 12); [Me2Si(NH-SiMe2)(2)N](3)(BNR)(3) (13); (Me2Si-N)(3) (B(NR-BF)(2)NR)(3) (14); (R = Me: 8, 11, 13); (R = Et: 9, 12, 14); 8 reacts with n-BuLi under substitution of the fluorine by n-C4H9 (10). The isomerization of the cyclotri- to the cyclodisilazane in the reaction of the dilithiated (Si-N)(3) ring with 2 (Me3CN-BF)(3) has kinetical reasons. Me3CN(BF-NCMe3)(2)B-NHSiMe2-(N-SiMe2)(2)- B(CMe3N-BF)(2)NCMe3 (15) is formed. Mono- and dilithiated (Me2Si-NH)(4) reacts with (FB-NEt)(3) in a molar ratio 1:1 and 1:2 to give the exptected mono- and disubstituted cyclotetrasilazanes, the isomeric cyclodisilazane, [Me3CN(BF-NCMe3)(2)B-NHSiMe2-N-SiMe2](2) (18) is obtained in the reaction with (Me3CN-BF)(3) in a molar ratio 1:2. Lithium-bis(trimethylsilyl)amide substitutes successively at the (FB-NEt)(3) one or two fluorine atoms. EtN(BF-NEt)(2)B-N(SiMe3)(2) (19) and FB(NEt-B)(2)[N(SiMe3)(2)](2)NEt (20) are formed. 20 reacts with (Me3Si)(2)NH to give Me3SiF and bis(3,5-bis(bis(trimethylsilyl)amino-2,4,6-triethyl)borazinyl)amine (21); [EtN(B-N(SiMe3)(2)NEt)(2)B](2)NH. The crystal structures of 1, 3, 6, 12 - 15, 18 and 21 are reported.
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