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1,1-二乙氧基环十二烷 | 957-17-5

中文名称
1,1-二乙氧基环十二烷
中文别名
——
英文名称
Cyclododecanone diethyl acetal
英文别名
1,1-diethoxycyclododecane;Cyclododecanon-diethylacetal;Cyclododecanon-diethylketal;Cyclododecanondiethylketal
1,1-二乙氧基环十二烷化学式
CAS
957-17-5
化学式
C16H32O2
mdl
——
分子量
256.429
InChiKey
XMQLLEROFXPBDO-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

  • 保留指数:
    1896;1908.4;1930.3

计算性质

  • 辛醇/水分配系数(LogP):
    5.6
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:b56b4830e1e627e8934382976e438d60
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Nitrosation in organic chemistry. Nitrosolysis, a novel carbon-carbon bond cleavage effected through nitrosation. Nitrosolysis of ketones and ketone acetals
    摘要:
    DOI:
    10.1021/ja00446a031
  • 作为产物:
    描述:
    乙醇环十二酮原甲酸三乙酯 作用下, 反应 3.0h, 以98%的产率得到1,1-二乙氧基环十二烷
    参考文献:
    名称:
    由酮制备二甲基和二乙基乙缩醛以及由环状β-二酮制备β-酮烯醇醚中的甲苯磺酸铁(III)
    摘要:
    摘要 描述了一种使用 Fe(OTs)3 作为催化剂将酮转化为相应的二甲基和二乙基缩醛以及将环状 β-二酮转化为 β-酮烯醇醚的有效方法。
    DOI:
    10.1080/00397910802219361
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文献信息

  • 2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO), N-Bromosuccinimide (NBS) and Bromine as Efficient Catalysts for Dithioacetalization and Oxathioacetalization of Carbonyl Compounds and Transdithioacetalization Reactions
    作者:Nasser Iranpoor、Habib Firouzabadi、Hamid Reza Shaterian、M. A. Zolfigol
    DOI:10.1080/10426500211712
    日期:2002.5.1
    6-tetrabromo-2,5-cyclohexadienone (TABCO), N-bromosuccinimide (NBS), and bromine as efficient catalysts for conversion of carbonyl compounds to their cyclic and acyclic dithioacetals and 1,3-oxathiolanes under mild reaction conditions are described. These catalysts are also used for efficient transdithioacetalization of acetals, diacetals, ketals, acylals, enamines, hydrazones, and oximes with high
    使用 2,4,4,6-四溴-2,5-环己二烯酮 (TABCO)、N-溴代琥珀酰亚胺 (NBS) 和溴作为有效催化剂将羰基化合物转化为环状和无环二硫缩醛和 1,3-描述了在温和反应条件下的硫杂环戊烷。这些催化剂还用于在硫醇存在下以高产率有效地将缩醛、二缩醛、缩酮、酰基、烯胺、腙和肟转二硫缩醛。
  • Lymph-absorbable aryl substituted imidazole derivatives
    申请人:Shionogi & Co., Ltd.
    公开号:US06054591A1
    公开(公告)日:2000-04-25
    A compound of the formula (I): ##STR1## salt thereof, or hydrate thereof which can effectively be absorbed from the lymph vessel in the intestinal tract and transferred to the lymph node in a high concentration is provided.
    公式(I)的化合物:##STR1##及其盐或水合物,可以有效地从肠道的淋巴管吸收,并以高浓度转移到淋巴结。
  • 2,4,4,6-Tetrabromo-2,5-cyclohexadienone (TABCO) as a Versatile, Efficient, and Chemoselective Catalyst for the Acetalization and Transacetalization of Carbonyl Compounds, the Preparation of Acetonides from Epoxides and Acylals (1,1-Diacetates) from Aldehydes
    作者:Habib Firouzabadi、Nasser Iranpoor、Hamid Reza Shaterian
    DOI:10.1246/bcsj.75.2195
    日期:2002.10
    The efficient and chemoselective preparation of acetals and ketals from carbonyl compounds, transacetalization reactions, the conversion of epoxides to acetonides, and the preparation of acylals from aldehydes in the presence of catalytic amounts of 2,4,4,6-tetrabromo-2,5-cyclohexadienone (TABCO) are described.
    介绍了在催化量的2,4,4,6-四溴-2,5-环己二烯酮(TABCO)存在下,从羰基化合物高效且化学选择性地制备缩醛和缩酮、缩醛交换反应、环氧化合物转化为乙缩醛以及醛制备酰缩醛的方法。
  • A simple, one-flask transformation of ketones to N-methyl lactams
    作者:Robert V. Hoffman、James M. Salvador
    DOI:10.1016/s0040-4039(00)74345-0
    日期:1991.11
    A one-flask conversion of cyclic ketones to N-methyl lactams is described. Reaction of the ketone with triethylorthoformate generates an acetal which is reacted in situ with N-(((p-nitrobenzene)sulfonyl)oxy methylamine 2a(CH3NH-OSO2C6H4NO2). Dealkylation of the resulting O-ethyl imidate with sodium iodide gives the lactam. A variety of lactams, including macrocyclic lactams, are produced simply and
    描述了环状烧瓶到N-甲基内酰胺的单烧瓶转化。酮与原甲酸三乙酯反应生成缩醛,该缩醛与N-(((对硝基苯)磺酰基)氧基甲胺2a(CH 3 NH-OSO 2 C 6 H 4 NO 2)原位反应。亚胺酸乙酯与碘化钠制得内酰胺,可以简单,高收率地生产各种内酰胺,包括大环内酰胺。
  • Highly Efficient Transdithioacetalization of Acetals Catalyzed by Silica Chloride
    作者:Habib Firouzabadi、Nasser Iranpoor、Babak Karimi、Hassan Hazarkhani
    DOI:10.1055/s-2000-6483
    日期:2000.2
    A modified procedure for the preparation of a silica chloride with higher chloride capacity than that reported is described. Moreover, this silica chloride was found to be an effective catalyst for chemoselective and highly efficient transdithioacetalization of different classes of acetals.
    描述了一种改良的制备方法,用于获得氯化硅,其氯容量高于已报道的水平。此外,这种氯化硅被发现是一种有效的催化剂,适用于各类缩醛的选择性高效反二硫缩醛化反应。
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