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1-Hydroxy-3-thiophen-2-ylpropan-2-one | 1167435-41-7

中文名称
——
中文别名
——
英文名称
1-Hydroxy-3-thiophen-2-ylpropan-2-one
英文别名
——
1-Hydroxy-3-thiophen-2-ylpropan-2-one化学式
CAS
1167435-41-7
化学式
C7H8O2S
mdl
——
分子量
156.205
InChiKey
DRKSJTLRLVOILY-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):
    0.6
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    65.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    盐酸 作用下, 以 四氢呋喃 为溶剂, 反应 0.5h, 生成 1-Hydroxy-3-thiophen-2-ylpropan-2-one
    参考文献:
    名称:
    Microwave-Assisted One-Carbon Chain Extension in the Preparation of Terminal α-Hydroxy Ketones
    摘要:
    The microwave-assisted synthesis of terminal -hydroxy ketones from acid chlorides and tris(trimethylsiloxy)ethylene in the presence of triethylamine is reported. The use of triethylamine had several advantages in the reaction: it increased the reactivity of the acid chloride, acted as a scavenger of the HCl that was produced in the reaction, protected the silylated enol from decomposition, and made the excess use of the silyl reagent unnecessary. Mechanistic effects of triethylamine are discussed. Effects of various base additives, reaction temperatures, reaction times, and solvents in the reaction are compared.
    DOI:
    10.1080/00397910802632589
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文献信息

  • Organic metal compound and process for preparing optically-active alcohols using the same
    申请人:Miki Takashi
    公开号:US20090062573A1
    公开(公告)日:2009-03-05
    The present invention provides an asymmetric reduction catalyst effective in preparing optically-active alcohol compounds having various functional groups, and a process for preparing optically-active alcohol compounds using said asymmetric reduction catalyst. The organic metal compound of the present invention is represented by the following general formula (1): wherein R 1 and R 2 may be mutually identical or different, and are an alkyl group, a phenyl group, a naphthyl group, a cycloalkyl group, or an alicyclic ring formed by binding R 1 and R 2 , which may have a substituent; R 3 is a hydrogen atom or an alkyl group; Cp is a cyclopentadienyl group, which may have a substituent, bound to M 1 via a π bond; X 1 is a halogen atom or a hydrido group; M 1 is rhodium or iridium; and * denotes asymmetric carbon.
    本发明提供了一种在制备具有各种官能团的光学活性醇化合物中有效的非对称还原催化剂,以及使用所述非对称还原催化剂制备光学活性醇化合物的方法。 本发明的有机属化合物由以下通式(1)表示: 其中R1和R2可以相互相同或不同,并且是烷基、苯基、基、环烷基或由R1和R2结合形成的脂肪环环,其中可能含有取代基;R3是氢原子或烷基;Cp是环戊二烯基,可能含有取代基,通过π键与M1结合;X1是卤素原子或氢化物基团;M1是;*表示不对称碳。
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