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4-苯基氨基-3-戊烯-2-酮 | 26567-78-2

中文名称
4-苯基氨基-3-戊烯-2-酮
中文别名
4-苯氨基-3-戊烯-2-酮
英文名称
(Z)-4-(phenylamino)-3-penten-2-one
英文别名
(Z)-4-(phenylamino)pent-3-en-2-one;4-(phenylamino)pent-3-en-2-one;(3Z)-4-anilinopent-3-en-2-one;4-Phenylaminopent-3-EN-2-one;(Z)-4-anilinopent-3-en-2-one
4-苯基氨基-3-戊烯-2-酮化学式
CAS
26567-78-2
化学式
C11H13NO
mdl
——
分子量
175.23
InChiKey
JLTWHWBUKGOPLH-HJWRWDBZSA-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

  • 熔点:
    48-52 °C (lit.)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    29.1
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 安全说明:
    S26,S36
  • 危险类别码:
    R36/37/38
  • WGK Germany:
    3

SDS

SDS:f49de5fcceae0dea1ba9d20c5ae51bb7
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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:
    4-苯基氨基-3-戊烯-2-酮对甲苯磺酰叠氮 、 sodium hydride 作用下, 以 乙腈 为溶剂, 反应 24.0h, 以40%的产率得到1-(5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)ethanone
    参考文献:
    名称:
    一种新的高效制备1,2,3-三唑的方法
    摘要:
    通过与β-氨基-α,β-不饱和酮或酯以及甲苯磺酰基或甲磺酰基叠氮化物试剂进行重氮转移反应,可以容易地以中等至良好的产率获得1,2,3-三唑。在这种方法中,三唑环的氮原子N-2和N-3衍生自重氮转移试剂,氮原子N-1衍生自适当的烯胺。
    DOI:
    10.1016/s0040-4039(97)01137-4
  • 作为产物:
    描述:
    4-(1-imidazolyl)-3-penten-2-one 在 三乙胺 作用下, 以 甲醇 为溶剂, 反应 2.0h, 生成 4-苯基氨基-3-戊烯-2-酮
    参考文献:
    名称:
    Kashima, C.; Tajima, T.; Shimizu, M., Journal of Heterocyclic Chemistry, 1982, vol. 19, p. 1325 - 1328
    摘要:
    DOI:
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文献信息

  • Highly efficient and facile synthesis of β-enaminones catalyzed by diphenylammonium triflate
    作者:Ting-Ting Zhao、Jiang-Long Song、Feng-Qing Hong、Jian-Sheng Xia、Jian-Jun Li
    DOI:10.1007/s11696-019-00838-2
    日期:2019.11
    The catalytic performance of diphenylammonium triflates as an organocatalyst in the synthesis of β-enaminones from various substituted β-diketones and amides (or amines) were evaluated. A wide range of β-enaminones were efficiently synthesized in good to excellent yields under mild reaction conditions. Applying diphenylammonium triflate (DPAT) as catalyst makes this protocol cost-effective, low corrosive and easy to handle.
    二苯胺三氟甲磺酸盐作为有机催化剂在合成各种取代β-二酮和酰胺(或胺)的β-烯胺酮中的催化性能得到了评估。在温和的反应条件下,广泛范围的β-烯胺酮以良好至优异的产率有效合成。将二苯胺三氟甲磺酸盐(DPAT)作为催化剂使得这一方案成本效益高、腐蚀性低且易于操作。
  • Efficient Synthetic Method for β-Enamino Esters Catalyzed by Yb(OTf)3 under Solvent-Free Conditions
    作者:Ravi Varala、Sreelatha Nuvula、Srinivas R. Adapa
    DOI:10.1071/ch06239
    日期:——
    esters have been synthesized in moderate to excellent yields by reacting 1,3-dicarbonyl compounds with amines in the presence of catalytic amounts of Yb(OTf)3 (2 mol%). The reaction proceeds smoothly at ambient temperature under solvent-free conditions. The catalyst can be recovered and reused.
    在催化量的 Yb(OTf)3 (2 mol%) 存在下,通过 1,3-二羰基化合物与胺反应,以中等至极好的产率合成了多种 β-烯氨基酯。该反应在环境温度下在无溶剂条件下顺利进行。催化剂可以回收再利用。
  • [EN] NITROGEN TITANIUM COMPLEX, CATALYTIC SYSTEM COMPRISING SAID NITROGEN TITANIUM COMPLEX AND PROCESS FOR THE (CO)POLYMERIZATION OF CONJUGATED DIENES<br/>[FR] COMPLEXE D'AZOTE TITANE, SYSTÈME CATALYTIQUE COMPRENANT LEDIT COMPLEXE D'AZOTE TITANE ET PROCÉDÉ DE (CO)POLYMÉRISATION DE DIÈNES CONJUGUÉS
    申请人:VERSALIS SPA
    公开号:WO2017017203A1
    公开(公告)日:2017-02-02
    Nitrogen titanium complex having general formula (I) or (II), wherein: - R1 represents a hydrogen atom; or is selected from linear or branched C1-C20 alkyl groups, preferably C1-C15, optionally halogenated, cycloalkyl groups optionally substituted, aryl groups optionally substituted; - R2, R3, R4 and R5, identical or different, represent a hydrogen atom; or are selected from linear or branched C1-C20 alkyl groups, preferably C1-C15, optionally halogenated, cycloalkyl groups optionally substituted, aryl groups optionally substituted, nitro groups, hydroxyl groups, amino groups; - Y represents a NH-R6 group wherein R6 represents a hydrogen atom, or is selected from linear or branched C1-C20 alkyl groups, preferably C1-C15, optionally halogenated, cycloalkyl groups optionally substituted, aryl groups optionally substituted; or a N-R7 group wherein R7 is selected from linear or branched C1-C20 alkyl groups, preferably C1-C15, optionally halogenated, cycloalkyl groups optionally substituted, aryl groups optionally substituted; - X1, X 2, X 3 and X 4, identical or different, represent a halogen atom, such as, for example, chlorine, bromine, iodine, preferably chlorine; or are selected from linear or branched C1 -C20 alkyl groups, preferably C1-C15, -OCOR8 or -OR8 groups wherein R8 is selected from linear or branched C1-C20 alkyl groups, preferably C1-C15; or one of X1, X2 and X3 is selected from ethers, such as,for example, diethylether, tetrahydrofuran (THF), dimethoxyethane, preferably tetrahydrofuran (THF); - n is 1 in the case wherein Y represents a NH-R6 group wherein R6 has the same meanings reported above; or is 0 in the case wherein Y represents a N-R7 group wherein R7 has the same meanings reported above, or in the case wherein one of X1, X2 and X3 is selected from ethers; - R'1, R' 2, R'3, R'4, R'5, R'6 and R'7, identical or different, represent a hydrogen atom; or are selected from linear or branched C1-C20 alkyl groups, preferably C1-C15, optionally halogenated, cycloalkyl groups optionally substituted, aryl groups optionally substituted; - X'1 and X'2, identical or different, represent a halogen atom such as, for example, chlorine, bromine, iodine, preferably chlorine; or are selected from linear or branched C1-C20 alkyl groups, preferably C1-C15, -OCOR'8 groups or -OR'8 groups wherein R' 8 is selected from linear or branched C1-C20 alkyl groups, preferably C1-C15; - Y' is selected from ethers such as, for example,diethylether, tetrahydrofuran (THF), dimethoxyethane, preferably is tetrahydrofuran (THF); or Y' represents a group having general formula (III), wherein R'1, R' 2, R'3, R'4, R'5, R'6 and R'7, have the same meanings as reported above; - m is 0 or 1. Said nitrogen titanium complex having general formula (I) or (II) can be advantageously used in a catalytic system for the (co)polymerization of conjugated dienes.
    氮钛配合物的一般化学式为(I)或(II),其中:- R1代表氢原子;或者选自线性或支链的C1-C20烷基,优选C1-C15,可选择卤代,环烷基可选择取代,芳基可选择取代;- R2、R3、R4和R5,相同或不同,代表氢原子;或选自线性或支链的C1-C20烷基,优选C1-C15,可选择卤代,环烷基可选择取代,芳基可选择取代,硝基,羟基,氨基;- Y代表NH-R6基团,其中R6代表氢原子,或选自线性或支链的C1-C20烷基,优选C1-C15,可选择卤代,环烷基可选择取代,芳基可选择取代;或N-R7基团,其中R7选自线性或支链的C1-C20烷基,优选C1-C15,可选择卤代,环烷基可选择取代,芳基可选择取代;- X1、X2、X3和X4,相同或不同,代表卤素原子,例如氯、溴、碘,优选氯;或选自线性或支链的C1-C20烷基,优选C1-C15,-OCOR8或-OR8基团,其中R8选自线性或支链的C1-C20烷基,优选C1-C15;或X1、X2和X3中的一个选自醚类化合物,例如二乙醚、四氢呋喃(THF)、二甲氧基乙烷,优选四氢呋喃(THF);- n在Y代表NH-R6基团的情况下为1,其中R6具有上述相同含义;或在Y代表N-R7基团的情况下为0,其中R7具有上述相同含义,或在X1、X2和X3中的一个选自醚类化合物的情况下为0;- R'1、R'2、R'3、R'4、R'5、R'6和R'7,相同或不同,代表氢原子;或选自线性或支链的C1-C20烷基,优选C1-C15,可选择卤代,环烷基可选择取代,芳基可选择取代;- X'1和X'2,相同或不同,代表卤素原子,例如氯、溴、碘,优选氯;或选自线性或支链的C1-C20烷基,优选C1-C15,-OCOR'8基团或-OR'8基团,其中R'8选自线性或支链的C1-C20烷基,优选C1-C15;- Y'选自醚类化合物,例如二乙醚、四氢呋喃(THF)、二甲氧基乙烷,优选四氢呋喃(THF);或Y'代表具有一般化学式(III)的基团,其中R'1、R'2、R'3、R'4、R'5、R'6和R'7具有上述相同含义;- m为0或1。具有一般化学式(I)或(II)的氮钛配合物可优势地用于共轭二烯的催化系统中的(共)聚合。
  • Magnesium Perchlorate as Efficient Lewis Acid: A Simple and Convenient Route to 1,4-Dihydropyridines
    作者:Letizia Sambri、Giuseppe Bartoli、Krzysztof Babiuch、Marcella Bosco、Armando Carlone、Patrizia Galzerano、Paolo Melchiorre
    DOI:10.1055/s-2007-990839
    日期:——
    A new protocol for the synthesis of various 1,2,3,4-tetrasubstituted 1,4-dihydropyridines from enamino or carbonylic derivatives promoted by Mg(ClO4)2 is presented.
    本文提出了一种新的合成多种1,2,3,4-四取代-1,4-二氢吡啶的协议,该协议基于Mg(ClO4)2的促进作用,用于从烯胺或羰基衍生物进行合成。
  • Metal-organic frameworks containing nitrogen-donor ligands for efficient catalytic organic transformations
    申请人:The University of Chicago
    公开号:US10647733B2
    公开(公告)日:2020-05-12
    Metal-organic framework (MOFs) compositions based on nitrogen donor-based organic bridging ligands, including ligands based on 1,3-diketimine (NacNac), bipyridines and salicylaldimine, were synthesized and then post-synthetically metalated with metal precursors, such as complexes of first row transition metals. Metal complexes of the organic bridging ligands could also be directly incorporated into the MOFs. The MOFs provide a versatile family of recyclable and reusable single-site solid catalysts for catalyzing a variety of asymmetric organic transformations. The solid catalysts can also be integrated into a flow reactor or a supercritical fluid reactor.
    基于以氮为供体的有机桥联配体,包括基于1,3-二酮亚胺(NacNac)、联吡啶和柳酸亚胺的金属-有机框架(MOFs)组成物被合成,然后用金属前驱体如第一行过渡金属的络合物进行后合成金属化。有机桥联配体的金属络合物也可以直接并入MOFs中。MOFs提供了一个多功能的、可回收和可重复使用的单点固体催化剂家族,用于催化各种不对称有机转化。这些固体催化剂也可以集成到流动反应器或超临界流体反应器中。
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同类化合物

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