摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

diethyl (Z)-2-(2-nitrophenoxy)-2-butenedioate | 947394-77-6

中文名称
——
中文别名
——
英文名称
diethyl (Z)-2-(2-nitrophenoxy)-2-butenedioate
英文别名
diethyl 2-(2-nitrophenoxy)fumarate;diethyl (Z)-2-(2-nitrophenoxy)but-2-enedioate
diethyl (Z)-2-(2-nitrophenoxy)-2-butenedioate化学式
CAS
947394-77-6
化学式
C14H15NO7
mdl
——
分子量
309.276
InChiKey
QRQNDGCOARKRPS-XFXZXTDPSA-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):
    2.5
  • 重原子数:
    22
  • 可旋转键数:
    8
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    108
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    diethyl (Z)-2-(2-nitrophenoxy)-2-butenedioate 、 diethyl 2-(2-nitrophenoxy)maleate 在 氯磺酸 作用下, 反应 7.0h, 以0.1%的产率得到ethyl 8-nitro-4-oxo-4H-chromene-2-carboxylate
    参考文献:
    名称:
    EP1479667
    摘要:
    公开号:
  • 作为产物:
    描述:
    2-(2-Nitro-phenoxy)-3-(triphenyl-λ5-phosphanylidene)-succinic acid diethyl ester 在 silica gel 作用下, 反应 0.05h, 以33%的产率得到diethyl (Z)-2-(2-nitrophenoxy)-2-butenedioate
    参考文献:
    名称:
    Stereoselective Conversion of Stabilized Phosphorus Ylides to Dialkyl 2-(2-Nitro-phenoxy)-2-butenedioates in the Presense of Silica Gel in Solvent-Free Conditions
    摘要:
    Protonation of the highly reactive 1:1 intermediates, produced in the reaction between triphenylphosphine and dialkyl acetylenedicarboxylates, by 2-nitrophenol leads to vinyltriphenylphosphonium salts, which undergo a Michael addition reaction with a conjugate base to produce dialkyl 2-(2-nitro-phenoxy)-3-(triphenylphosphoranylidene)butanedioates. Silica-gel powder was found to catalyze the stereoselective conversion of dialkyl 2-(2-nitro-phenoxy)-3-(triphenylphosphoranylidene)butanedioates to dialkyl 2-(2-nitro-phenoxy)-2-butenedioates in solvent-free conditions under microwave (0.5 KW, 3 min) and thermal (90 degrees C, 60 min) conditions.
    DOI:
    10.1080/10426500600864346
点击查看最新优质反应信息

文献信息

  • Process for producing chromone compound
    申请人:Hibino Hiroaki
    公开号:US20050085664A1
    公开(公告)日:2005-04-21
    A process for producing a dicarboxylic acid compound represented by the formula (4): wherein R 1 and R 2 are the same or different and each represents lower alkyl and the wavy line indicates that this compound is the E- or Z-isomer or a mixture of them, characterized by reacting a compound represented by the formula (2): wherein R 1 , R 2 and the wavy line have the same meanings as the above, and one of X 2 and X 3 represents hydrogen and the other represents halogen, with nitrophenol represented by the formula (3): in the presence of a base; a process for producing a nitrochromone compound represented by the formula (5): wherein R 1 has the same meaning as the above, characterized by reacting the dicarboxylic acid compound or carboxylic acid thereof with an acid; a process for producing an aminochromone compound which comprises reducing the nitrochromone compound; and a process for producing an amidochromone compound which comprises acylating the aminochromone compound are provided.
    提供一种制备式(4)的二羧酸化合物的方法,其中R1和R2相同或不同,每个代表低级烷基,波浪线表示该化合物是E或Z异构体或它们的混合物,其特征在于将式(2)的化合物与硝基酚在碱的存在下反应,式中R1、R2和波浪线的含义与上述相同,X2和X3中的一个代表氢,另一个代表卤素;提供一种制备式(5)的硝基香豆素化合物的方法,其中R1的含义与上述相同,其特征在于将二羧酸化合物或其羧酸与酸反应;提供一种制备氨基香豆素化合物的方法,其包括还原硝基香豆素化合物;以及提供一种制备酰胺香豆素化合物的方法,其包括酰化氨基香豆素化合物。
  • PROCESS FOR PRODUCING CHROMONE COMPOUND
    申请人:Sumitomo Chemical Company, Limited
    公开号:EP1479667A1
    公开(公告)日:2004-11-24
    A process for producing a dicarboxylic acid compound represented by the formula (4): wherein R1 and R2 are the same or different and each represents lower alkyl and the wavy line indicates that this compound is the E- or Z-isomer or a mixture of them, characterized by reacting a compound represented by the formula (2): wherein R1, R2 and the wavy line have the same meanings as the above, and one of X2 and X3 represents hydrogen and the other represents halogen, with nitrophenol represented by the formula (3): in the presence of a base; a process for producing a nitrochromone compound represented by the formula (5): wherein R1 has the same meaning as the above, characterized by reacting the dicarboxylic acid compound or carboxylic acid thereof with an acid; a process for producing an aminochromone compound which comprises reducing the nitrochromone compound; and a process for producing an amidochromone compound which comprises acylating the aminochromone compound are provided.
    一种生产由式(4)代表的二羧酸化合物的工艺: 其中 R1 和 R2 相同或不同,且各自代表低级烷基,波浪线表示该化合物为 E-或 Z-异构体或它们的混合物,其特征在于使式(2)所代表的化合物反应: 其中 R1、R2 和波浪线的含义与上述相同,X2 和 X3 中的一个代表氢,另一个代表卤素: 在碱存在下;生产式(5)代表的硝基色酮化合物的工艺: 其中 R1 的含义与上述相同,其特征在于使二羧酸化合物或其羧酸与酸反应;提供了一种生产氨基色素化合物的工艺,该工艺包括还原硝基色素化合物;以及一种生产氨基色素化合物的工艺,该工艺包括酰化氨基色素化合物。
  • Process for Producing Chromone Compound
    申请人:Sumitomo Chemical Company, Limited
    公开号:EP2105431A1
    公开(公告)日:2009-09-30
    A process for producing a dihalosuccinic acid compound in which the proportion of a threo-dihalosuccinic acid compound is 70% or higher, which comprises adding a maleic acid compound to a halogenating agent.
    一种生产二卤代琥珀酸化合物的工艺,其中三卤代二卤代琥珀酸化合物的比例为 70% 或更高,该工艺包括在卤化剂中加入马来酸化合物。
  • US7094914B2
    申请人:——
    公开号:US7094914B2
    公开(公告)日:2006-08-22
  • EP1479667
    申请人:——
    公开号:——
    公开(公告)日:——
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐