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1,1,3,3-Tetrabutyl-1,3-dimethoxydistannoxan | 5926-85-2

中文名称
——
中文别名
——
英文名称
1,1,3,3-Tetrabutyl-1,3-dimethoxydistannoxan
英文别名
tetra butyl dimethoxide distannoxane;1,3-dimethoxy-1,1,3,3-tetrabutyldistannoxane;bis(dibutylmethoxytin) oxide;metal methoxide from dibutiltin oxide and methanol;1,1,3,3-tetrabutyl-1,3-dimethoxy-distannoxane;dibutyl-[dibutyl(methoxy)stannyl]oxy-methoxystannane
1,1,3,3-Tetrabutyl-1,3-dimethoxydistannoxan化学式
CAS
5926-85-2
化学式
C18H42O3Sn2
mdl
——
分子量
543.95
InChiKey
WGXIHTBBHDMEFD-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

物化性质

  • 沸点:
    399.9±25.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.38
  • 重原子数:
    23
  • 可旋转键数:
    16
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:d96a188b29d3f4a01808e3f989c9fdb1
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反应信息

  • 作为反应物:
    描述:
    1,1,3,3-Tetrabutyl-1,3-dimethoxydistannoxan溶剂黄146 作用下, 以 二氯甲烷 为溶剂, 生成 1-acetoxy-3-methoxy-1,1,3,3-tetrabutyldistannoxane
    参考文献:
    名称:
    Gross, David C., Inorganic Chemistry, 1989, vol. 28, # 12, p. 2355 - 2359
    摘要:
    DOI:
  • 作为产物:
    描述:
    1,1,3,3-tetrabutyl-1,3-dimethoxydistannoxane 以 甲醇 为溶剂, 生成 1,1,3,3-Tetrabutyl-1,3-dimethoxydistannoxan
    参考文献:
    名称:
    Di-n-butyltin(IV)-catalyzed dimethyl carbonate synthesis from carbon dioxide and methanol: An in situ high pressure 119Sn{1H} NMR spectroscopic study
    摘要:
    The reactivity of five di-n-butyltin(IV) complexes, n-Bu2Sn(OR)(2) (1), n-Bu2SnO (3), [n-Bu2Sn(OR)](2)O (4), (n-Bu2SnO)(2)(CO2) (6) and (n-Bu2SnO)(6)[(n-Bu2SnOR)(2)(CO3)](2) (7) (R = CH3), with CO2, suggested as possible catalyst precursors and key-intermediates for the direct synthesis of dimethyl carbonate from carbon dioxide and methanol, has been investigated using high-pressure Sn-119{H-1} NMR (HP-NMR) spectroscopy. Four of the five precursors studied, i.e. 3, 4, 6 and 7 give rise to an identical Sn-119{H-1} NMR pattern which can be explicitly attributed to the fingerprint of the dimeric form of the 1-methoxy-3-methylcarbonatotetrabutyldistannoxane {5}(2). However, with 1, a new pair of signals is observed in addition to the characteristic Sn-119{H-1} NMR resonances of the dimeric hemicarbonato species {2}(2) and {5}(2), which can be attributed to the in situ formation of an unprecedented species suggested to be the trinuclear carbonato di-n-butyltin(IV) complex, 8. (C) 2011 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2011.02.010
  • 作为试剂:
    描述:
    甲醇二氧化碳1,1,3,3-Tetrabutyl-1,3-dimethoxydistannoxandiphenylammonium triflate 2,2-二甲氧基丙烷 作用下, 180.0 ℃ 、30.4 MPa 条件下, 反应 24.0h, 以34%的产率得到碳酸二甲酯
    参考文献:
    名称:
    WO2006/109775
    摘要:
    公开号:
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文献信息

  • Process for synthesizing sucrose derivatives by regioselective reaction
    申请人:Noramco, Inc.
    公开号:US04950746A1
    公开(公告)日:1990-08-21
    Sucrose is reacted with a 1,3-di(hydrocarbyloxy)-1,1,3,3-tetra(hydrocarbyl)distannoxane to produce a 1,3-di-(6-O-sucrose)-1,1,3,3-tetra(hydrocarbyl)distannoxane, which can be acylated to produce a sucross-6-ester.
    蔗糖与1,3-二(羟烷氧基)-1,1,3,3-四(烷基)二锡氧烷反应,生成1,3-二-(6-O-蔗糖基)-1,1,3,3-四(烷基)二锡氧烷,可以酰化成蔗糖-6-酯。
  • METHOD FOR PRODUCING A CARBONIC ESTER
    申请人:Asahi Kasei Chemicals Corporation
    公开号:EP1460056B1
    公开(公告)日:2011-10-05
  • Diol-tin ketal as effective catalyst in the tin mediated benzoylation of polyols
    作者:Ezio Fasoli、Antonio Caligiuri、Stefano Servi、Davide Tessaro
    DOI:10.1016/j.molcata.2005.08.042
    日期:2006.2
    The monobenzoylation of 1-phenyl-1,2-ethanediol in the presence of different tin reagent has been studied. The stannylene ketal of 1-phenyl-1,2-ethanediol has been prepared and used as a catalyst or generated in situ by exchange with other mixed tin ketals. In either case, the acylation occurs rapidly with 2 mol% of the catalyst with the known selectivity. These experiments clearly establish the catalytic nature of the acylation reaction. (c) 2005 Elsevier B.V. All rights reserved.
  • Gross, David C., Inorganic Chemistry, 1989, vol. 28, # 12, p. 2355 - 2359
    作者:Gross, David C.
    DOI:——
    日期:——
  • Di-n-butyltin(IV)-catalyzed dimethyl carbonate synthesis from carbon dioxide and methanol: An in situ high pressure 119Sn{1H} NMR spectroscopic study
    作者:Gábor Laurenczy、Michel Picquet、Laurent Plasseraud
    DOI:10.1016/j.jorganchem.2011.02.010
    日期:2011.5
    The reactivity of five di-n-butyltin(IV) complexes, n-Bu2Sn(OR)(2) (1), n-Bu2SnO (3), [n-Bu2Sn(OR)](2)O (4), (n-Bu2SnO)(2)(CO2) (6) and (n-Bu2SnO)(6)[(n-Bu2SnOR)(2)(CO3)](2) (7) (R = CH3), with CO2, suggested as possible catalyst precursors and key-intermediates for the direct synthesis of dimethyl carbonate from carbon dioxide and methanol, has been investigated using high-pressure Sn-119H-1} NMR (HP-NMR) spectroscopy. Four of the five precursors studied, i.e. 3, 4, 6 and 7 give rise to an identical Sn-119H-1} NMR pattern which can be explicitly attributed to the fingerprint of the dimeric form of the 1-methoxy-3-methylcarbonatotetrabutyldistannoxane 5}(2). However, with 1, a new pair of signals is observed in addition to the characteristic Sn-119H-1} NMR resonances of the dimeric hemicarbonato species 2}(2) and 5}(2), which can be attributed to the in situ formation of an unprecedented species suggested to be the trinuclear carbonato di-n-butyltin(IV) complex, 8. (C) 2011 Elsevier B. V. All rights reserved.
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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