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1,2-divinylcyclododecan-1-ol | 35951-27-0

中文名称
——
中文别名
——
英文名称
1,2-divinylcyclododecan-1-ol
英文别名
1,2-divinylcyclododecanol;1,2-Divinyl-cyclododecan-1-ol;1,2-Divinylcyclododeanol-(1);1,2-Divinylcyclododecanol-1;1,2-Divinyl-cyclododecanol;Cyclododecanol, 1,2-diethenyl-;1,2-bis(ethenyl)cyclododecan-1-ol
1,2-divinylcyclododecan-1-ol化学式
CAS
35951-27-0
化学式
C16H28O
mdl
——
分子量
236.398
InChiKey
MHRGVXURTWTWEO-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:
    313.0±21.0 °C(Predicted)
  • 密度:
    0.945±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.6
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • Transposition oxy-cope assistee par le trifluoroacetate mercurique en quantite stoechiometrique et en quantite catalytique
    作者:Norbert Bluthe、Max Malacria、Jacques Gore
    DOI:10.1016/0040-4020(84)85011-5
    日期:1984.1
    Tertiary 1,5-hexadien-3-ols are transformed at room temperature into δ-ethylenic ketones in 35-90%, yields under two sets of conditions: treatment with one molar equivalent of mercuric trifluoroacetate followed by demercuration of the intermediate α-mercuro ketone with sodium borohydride; and treatment with 0.2 molar equivalent of t of lithium trifluoroacetate or trifluorométhansulfonate. The reactions
    在室温下,将1,5-己二烯-3-醇叔化成35-90%的δ-乙烯酮,在两种条件下收率:用一摩尔当量的三氟乙酸汞处理,然后使中间的α-水银脱汞酮与硼氢化钠;用0.2摩尔当量的三氟乙酸锂或三氟甲磺酸锂处理。反应是高度立体选择性的,酮的E异构体占产物的80-95%。在第二条件下观察到最高的选择性。
  • Process for the preparation of 8-ethylenic carbonyl compounds
    申请人:Rhone-Poulenc Sante
    公开号:US04421934A1
    公开(公告)日:1983-12-20
    Process for the preparation of .delta.-ethylenic carbonyl compounds of the formula (I) by the oxy-Cope rearrangement of a diethylenic alcohol of the formula (II), in the presence of a mercuric salt: in formulae (I) and (II), R.sub.1, R.sub.2, R.sub.4, R.sub.5 and R.sub.6, which are identical or different, represent a hydrogen atom or an acyclic hydrocarbon radical and R.sub.3 represents an acyclic hydrocarbon radical, it being understood that R.sub.1 and R.sub.3 can together form a trimethylene radical, or alternatively that R.sub.3 and R.sub.4 can together form an alkylene radical containing 3 to 20 carbon atoms. ##STR1##
    通过二乙烯醇的氧Cope重排反应,存在汞盐的情况下,制备公式(I)的.delta.-烯醇酮化合物的过程:在公式(I)和(II)中,R.sub.1、R.sub.2、R.sub.4、R.sub.5和R.sub.6相同或不同,表示氢原子或非环烃基,而R.sub.3表示非环烃基,其中R.sub.1和R.sub.3可以一起形成三甲基基团,或者R.sub.3和R.sub.4可以一起形成含有3至20个碳原子的烷基基团。## STR1##
  • Process and apparatus for production of 5-cyclohexadecen-1-one
    申请人:Takasago International Corporation
    公开号:EP0955285A1
    公开(公告)日:1999-11-10
    This invention relates to a process for producing 5-cyclohexadecen-1-one continuously from 1,2-divinylcyclododecanol in a short time in an efficient manner without no side reaction. In the process, 1,2-divinylcyclododecanol as starting material is supplied from a raw material container 1 by a fixed delivery pump 2 to a flash unit 3 which is vacuumed to 5 mm Hg (666.5 Pa) or less by a vacuum pump 8 and is heated and 1,2-divinylcyclododecanol which is flashed in the flash unit is supplied to a reactor 4 which is heated to 400 to 650°C and vacuumed to 5 mm Hg (666.5 Pa) or less whereby 1,2-divinylcyclododecanol is converted into 5-cyclohexadecen-1-one. The reaction product is discharged from the top of the reactor and is cooled to recover the objective 5-cyclohexadecen-1-one in the recovery container 6. The reduction in the pressure of the apparatus is preferably performed by a vacuum pump 8 via a hydrochloric acid trap 7 comprising, for example, sodium methylate/methanol cooled to -78 to -100°C.
    本发明涉及一种以 1,2-二乙烯基环十二醇为原料在短时间内连续生产 5-环 十六烯-1-酮的工艺,生产过程高效且无副作用。在该工艺中,1,2-二乙烯基环十二醇作为起始原料由固定输送泵 2 从原料容器 1 输送到闪蒸装置 3,闪蒸装置 3 通过真空泵抽真空至 5 毫米汞柱(666.闪蒸单元中闪蒸的 1,2-二乙烯基环十二醇被送入反应器 4,反应器 4 被加热至 400 至 650°C,真空度为 5 mm Hg (666.5 Pa) 或更低,1,2-二乙烯基环十二醇由此转化为 5-环十六烯-1-酮。反应产物从反应器顶部排出,冷却后在回收容器 6 中回收目标 5-环十六烯-1-酮。设备的减压最好由真空泵 8 通过盐酸捕集器 7 来完成,盐酸捕集器 7 包括冷却至 -78 至 -100°C 的甲酸钠/甲醇等。
  • BLUTHE, N.;MALACRIA, M.;GORE, J., TETRAHEDRON LETT., 1982, 23, N 41, 4263-4266
    作者:BLUTHE, N.、MALACRIA, M.、GORE, J.
    DOI:——
    日期:——
  • BLUTHE, N.;MALACRIA, M.;GORE, J., TETRAHEDRON, 1984, 40, N 17, 3277-3284
    作者:BLUTHE, N.、MALACRIA, M.、GORE, J.
    DOI:——
    日期:——
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