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7-Anilinooxy-1,4-dioxaspiro[4.5]decan-8-one | 702711-84-0

中文名称
——
中文别名
——
英文名称
7-Anilinooxy-1,4-dioxaspiro[4.5]decan-8-one
英文别名
——
7-Anilinooxy-1,4-dioxaspiro[4.5]decan-8-one化学式
CAS
702711-84-0
化学式
C14H17NO4
mdl
——
分子量
263.293
InChiKey
KAVBTTIIAFQRLE-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):
    1.7
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    56.8
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    7-Anilinooxy-1,4-dioxaspiro[4.5]decan-8-one 在 europioum(III) chloride 作用下, 以 乙醇 为溶剂, 反应 0.02h, 生成 7-Phenylamino-1,4-dioxa-spiro[4.5]dec-6-en-8-one 、 8-Phenylamino-1,4-dioxa-spiro[4.5]dec-8-en-7-one
    参考文献:
    名称:
    Metal-Induced Reactions ofO-Nitroso Aldol Products
    摘要:
    路易斯酸催化剂在δ-氨基氧基酮(O-亚硝基醛醇产物)的转化过程中发挥着重要作用。本文介绍了金属离子促进 O-亚硝基醛醇产物的三种不同反应。
    DOI:
    10.1055/s-2006-933123
  • 作为产物:
    描述:
    1-((1,4-dioxaspiro[4.5]dec-7-en-8-yl)oxy)-1,1,2,2,2-pentamethyldisilane 、 亚硝基苯 在 silver tetrafluoroborate 、 13-Phenoxy-10,16-diphenyl-12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaene 、 cesium fluoride 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 16.0h, 以85%的产率得到7-Anilinooxy-1,4-dioxaspiro[4.5]decan-8-one
    参考文献:
    名称:
    甲硅烷基烯醇醚的对映选择性O-亚硝基醛醇缩合反应。
    摘要:
    DOI:
    10.1002/anie.200705679
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文献信息

  • Process of making alpha-aminooxyketone/alpha-aminooxyaldehyde and alpha-hydroxyketone/alpha-hydroxyaldehyde compounds and a process making reaction products from cyclic alpha,beta-unsaturated ketone substrates and nitroso substrates
    申请人:Momiyama Norie
    公开号:US20070037973A1
    公开(公告)日:2007-02-15
    The present invention is directed to a process of making α-aminooxyketone and α-hydroxyketone compounds. The synthetic pathway generally involves reacting an aldehyde or ketone substrate and a nitroso substrate in the presence of a catalyst of the formula (IV): wherein X a —X c represent independently nitrogen, carbon, oxygen or sulfur and Z represents a 4 to 10-membered ring with or without a substituent and optionally a further step to convert the α-aminooxyketone compound formed to the α-hydroxyketone compound. The present invention results in α-aminooxyketone and α-hydroxyketone compounds with high enantioselectivity and high purity. The present invention is also directed to a catalytic asymmetric O-nitroso Aldol/Michael reaction. The substrates of this reaction are generally cyclic α,β-unsaturated ketone substrate and a nitroso substrate. This methodology generally involves reacting the cyclic α,β-unsaturated ketone substrate and the nitroso substrate in the presence of a proline-based catalyst, to provide a heterocyclic product.
    本发明涉及一种制备α-氨氧基酮和α-羟基酮化合物的方法。合成途径通常涉及在催化剂存在下反应醛或酮底物和亚硝基底物,所述催化剂的公式为(IV):其中Xa-Xc分别独立表示氮、碳、氧或硫,Z表示具有或不具有取代基的4到10个成员环,并可选择进一步步骤将形成的α-氨氧基酮化合物转化为α-羟基酮化合物。本发明的结果是具有高对映选择性和高纯度的α-氨氧基酮和α-羟基酮化合物。本发明还涉及一种催化不对称O-亚硝基Aldol/Michael反应。该反应的底物通常为环状α,β-不饱和酮底物和亚硝基底物。该方法通常涉及在脯氨酸基催化剂存在下反应环状α,β-不饱和酮底物和亚硝基底物,以提供杂环产物。
  • PROCESS OF MAKING ALPHA-AMINOOXYKETONE/ALPHA-AMINOOXYALDEHYDE AND ALPHA-HYDROXYKETONE/ALPHA-HYDROXYALDEHYDE COMPOUNDS AND A PROCESS MAKING REACTION PRODUCTS FROM CYCLIC ALPHA, BETA-UNSATURATED KETONE SUBSTRATES AND NITROSO SUBSTRATES
    申请人:Momiyama Norie
    公开号:US20100099915A1
    公开(公告)日:2010-04-22
    The present invention is directed to a process of making α-aminooxyketone and α-hydroxyketone compounds. The synthetic pathway generally involves reacting an aldehyde or ketone substrate and a nitroso substrate in the presence of a catalyst of the formula (IV): wherein X a —X c represent independently nitrogen, carbon, oxygen or sulfur and Z represents a 4 to 10-membered ring with or without a substituent and optionally a further step to convert the α-aminooxyketone compound formed to the α-hydroxyketone compound. The present invention results in α-aminooxyketone and α-hydroxyketone compounds with high enantioselectivity and high purity. The present invention is also directed to a catalytic asymmetric O-nitroso Aldol/Michael reaction. The substrates of this reaction are generally cyclic α,β-unsaturated ketone substrate and a nitroso substrate. This methodology generally involves reacting the cyclic α,β-unsaturated ketone substrate and the nitroso substrate in the presence of a proline-based catalyst, to provide a heterocyclic product.
    本发明涉及一种制备α-氨氧酮和α-羟基酮化合物的过程。合成路径通常涉及在催化剂的存在下反应醛或酮底物和亚硝基底物,催化剂的公式为(IV):其中Xa-Xc代表独立的氮、碳、氧或硫,Z代表具有或不具有取代基的4到10个成员环,并可选择进一步步骤将形成的α-氨氧酮化合物转化为α-羟基酮化合物。本发明产生了具有高对映选择性和高纯度的α-氨氧酮和α-羟基酮化合物。本发明还涉及一种催化不对称O-亚硝基Aldol/Michael反应。该反应的底物通常是环状α,β-不饱和酮底物和亚硝基底物。该方法通常涉及在脯氨酸基催化剂的存在下反应环状α,β-不饱和酮底物和亚硝基底物,以提供杂环产物。
  • PROCESS OF MAKING ALFA-AMINOOXYKETONE/ ALFA-AMINOOXYALDEHYDE AND ALFA-HYDROXYKETONE/ ALFA-HYDROXYALDEHYDE COMPOUNDS AND A PROCESS OF MAKING REACTION PRODUCTS FROM CYCLIC ALFA, BETA-UNSATURATED KETONE SUBSTRATES AND NITROSO SUBSTRATES
    申请人:Japan Science and Technology Agency
    公开号:EP1742905A2
    公开(公告)日:2007-01-17
  • US7872123B2
    申请人:——
    公开号:US7872123B2
    公开(公告)日:2011-01-18
  • US8252941B2
    申请人:——
    公开号:US8252941B2
    公开(公告)日:2012-08-28
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同类化合物

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