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methyl (1R)-1-fluoro-2-oxocyclohexane-1-carboxylate | 144462-29-3

中文名称
——
中文别名
——
英文名称
methyl (1R)-1-fluoro-2-oxocyclohexane-1-carboxylate
英文别名
——
methyl (1R)-1-fluoro-2-oxocyclohexane-1-carboxylate化学式
CAS
144462-29-3
化学式
C8H11FO3
mdl
——
分子量
174.172
InChiKey
RTUMZQUWNLXPOW-MRVPVSSYSA-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:
    211.9±40.0 °C(Predicted)
  • 密度:
    1.17±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.1
  • 重原子数:
    12
  • 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:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    4

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
  • 下游产品
    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:
    methyl (1R)-1-fluoro-2-oxocyclohexane-1-carboxylate 在 sodium tetrahydroborate 、 对甲苯磺酸 作用下, 以 甲醇 为溶剂, 反应 8.5h, 生成 [(1S)-1-fluoro-2,2-dimethoxycyclohexyl]methanol
    参考文献:
    名称:
    A novel enantioselective preparation of α-fluoro-β-keto acids
    摘要:
    A two-step method for the enantioselective preparation of alpha-fluorinated beta-keto acids from 1,3-dioxin-4-ones having l-menthone as the chiral auxiliary at the 2-position is described. The method consists of fluorination of the dioxinones by molecular fluorine and solvolytic cleavage of the acetal function.
    DOI:
    10.1016/s0957-4166(00)86035-8
  • 作为产物:
    描述:
    potassium carbonate 、 fluorine 作用下, 以 甲醇乙腈 为溶剂, 反应 30.0h, 生成 methyl (1R)-1-fluoro-2-oxocyclohexane-1-carboxylate
    参考文献:
    名称:
    A novel enantioselective preparation of α-fluoro-β-keto acids
    摘要:
    A two-step method for the enantioselective preparation of alpha-fluorinated beta-keto acids from 1,3-dioxin-4-ones having l-menthone as the chiral auxiliary at the 2-position is described. The method consists of fluorination of the dioxinones by molecular fluorine and solvolytic cleavage of the acetal function.
    DOI:
    10.1016/s0957-4166(00)86035-8
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文献信息

  • Enantioselective α-Fluorination and Chlorination of β-Ketoesters by Cobalt Catalyst
    作者:Motoi Kawatsura、Shunsuke Hayashi、Yuji Komatsu、Shuichi Hayase、Toshiyuki Itoh
    DOI:10.1246/cl.2010.466
    日期:2010.5.5
    We demonstrated the cobalt-catalyzed asymmetric α-fluorination and α-chlorination of β-ketoesters. Both reactions were achieved using a catalytic amount of Co(acac)2 with (R,R)-Jacobsen’s salen ligand; α-fluorinated or α-chlorinated products were thus obtained with a good enentioselectivity.
    我们展示了钴催化的不对称 α-氟化和 α-氯化 β-酮酯反应。这两个反应都是使用催化量的 Co(acac)2 与 (R,R)-Jacobsen's salen 配体实现的;从而以良好的烯选择性获得了 α-氟化或 α-氯化产物。
  • Asymmetric fluorination of β-keto esters catalyzed by chiral rare earth perfluorinated organophosphates
    作者:Shoko Suzuki、Hiroshi Furuno、Yasuo Yokoyama、Junji Inanaga
    DOI:10.1016/j.tetasy.2005.12.029
    日期:2006.2
    Novel chiral rare earth metal complexes bearing perfluorinated binaphthyl phosphate ligand RE[(R)-F8BNP](3) (RE = rare earth; F8BNP = 5,5',6,6',7,7'.8,8'-octafluoro-1,1'-binaphthyl-2,2-diyl phosphate) have been synthesized and used as a catalyst for the asymmetric electrophilic fluorination reaction of beta-keto esters. The use of Sc[(R)-F8BNP](3) catalyst in combination with 1-fluoropyridinium triflate (NFPY-OTf) as a fluorinating agent was found to give the desired alpha-fluoro-beta-keto esters in high chemical yields and enantiomeric excesses (up to 88% ee) under mild conditions. (c) 2006 Elsevier Ltd. All rights reserved.
  • A novel enantioselective preparation of α-fluoro-β-keto acids
    作者:Tomoyasu Iwaoka、Tomoko Murohashi、Masayuki Sato、Chikara Kaneko
    DOI:10.1016/s0957-4166(00)86035-8
    日期:1992.8
    A two-step method for the enantioselective preparation of alpha-fluorinated beta-keto acids from 1,3-dioxin-4-ones having l-menthone as the chiral auxiliary at the 2-position is described. The method consists of fluorination of the dioxinones by molecular fluorine and solvolytic cleavage of the acetal function.
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