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3,4-bis(3,4-dimethylphenyl)cyclobutane-1,2-dicarboxylic acid | 1246218-90-5

中文名称
——
中文别名
——
英文名称
3,4-bis(3,4-dimethylphenyl)cyclobutane-1,2-dicarboxylic acid
英文别名
(1S,2R,3S,4R)-3,4-bis(3,4-dimethylphenyl)cyclobutane-1,2-dicarboxylic acid
3,4-bis(3,4-dimethylphenyl)cyclobutane-1,2-dicarboxylic acid化学式
CAS
1246218-90-5
化学式
C22H24O4
mdl
——
分子量
352.43
InChiKey
YCWOLSZVTKLCRU-JVSBHGNQSA-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):
    4
  • 重原子数:
    26
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 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

反应信息

  • 作为产物:
    参考文献:
    名称:
    拥挤的1,8-双(4'-苯胺基)萘模板的立体控制光二聚化
    摘要:
    将1,8-二卤代萘与4-甲氧基-3-甲基苯基硼酸或4-乙酰氨基苯硼酸进行铃木交叉偶联,然后进行官能团转化,得到1,8-双(3'-甲基-4'-苯胺基)萘,16,和1,8-双(4'-苯胺基)萘21的总收率分别为65%和90%。这些拥挤的化合物显示出两个有利于立体选择性光二聚化的共价连接的肉桂酰基单元近端,平行排列的苯胺环表面。发现[2 + 2]环加成以高收率进行并且排他地形成顺式,反式,顺式-环丁烷-1,2-二羧酸。与肉桂酰氯和模板21形成酰胺然后进行光化学二聚和酸性水解,以总收率的69%生成10%的β-精氨酸。在EDC,UV辐射和裂解作用下,将21和(E)-3-(3,4-二甲基苯基)丙烯酸偶联,得到顺,反,顺-3,4-双(3,4-二甲基苯基)环丁烷-1,2-二羧酸26,收率60%。在这两种情况下,模板都是定量回收的。
    DOI:
    10.1021/jo101547w
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文献信息

  • Stereocontrolled Photodimerization with Congested 1,8-Bis(4′-anilino)naphthalene Templates
    作者:Marwan W. Ghosn、Christian Wolf
    DOI:10.1021/jo101547w
    日期:2010.10.1
    transformation gave 1,8-bis(3′-methyl-4′-anilino)naphthalene, 16, and 1,8-bis(4′-anilino)naphthalene, 21, in 65% and 90% overall yield, respectively. These congested compounds exhibit two cofacial aniline rings that favor a proximate, parallel arrangement of covalently attached cinnamoyl units suitable for stereoselective photodimerization. The [2 + 2]cycloaddition was found to proceed with high yield and
    将1,8-二卤代萘与4-甲氧基-3-甲基苯基硼酸或4-乙酰氨基苯硼酸进行铃木交叉偶联,然后进行官能团转化,得到1,8-双(3'-甲基-4'-苯胺基)萘,16,和1,8-双(4'-苯胺基)萘21的总收率分别为65%和90%。这些拥挤的化合物显示出两个有利于立体选择性光二聚化的共价连接的肉桂酰基单元近端,平行排列的苯胺环表面。发现[2 + 2]环加成以高收率进行并且排他地形成顺式,反式,顺式-环丁烷-1,2-二羧酸。与肉桂酰氯和模板21形成酰胺然后进行光化学二聚和酸性水解,以总收率的69%生成10%的β-精氨酸。在EDC,UV辐射和裂解作用下,将21和(E)-3-(3,4-二甲基苯基)丙烯酸偶联,得到顺,反,顺-3,4-双(3,4-二甲基苯基)环丁烷-1,2-二羧酸26,收率60%。在这两种情况下,模板都是定量回收的。
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同类化合物

3,4-双(4-羟基苯基)环丁烷-1,2-二羧酸 3,4-二苯基环丁烷-1,2-二羧酸 1-[2,3-二甲基-4-(2,4,5-三甲氧基苯基)环丁基]-2,4,5-三甲氧基苯 (2,3,4-三苯基环丁基)苯 DL-(1R,2R,3S,4S)-3,4-bis(4-methoxyphenyl)cyclobutane-1,2-dicarboxylic acid tetrakis-1,2,3,4-(4’- carboxyphenyl)cyclobutane 3,3'-dinitro-β-truxinic acid diphenyl 3,4-diphenylcyclobutane-1,2-dicarboxylate DL-(1R,2R,3S,4S)-diphenyl 3,4-diphenylcyclobutane-1,2-dicarboxylate 3,4-bis(2-hydroxy-5-methylphenyl)cyclobutane-1,2-dicarboxylic acid N-(n-pentyl)-3β,4β-bis(3',4'-dimethoxyphenyl)-1α,2α-cyclobutanedicarboximide trans-1,2-diphenylbicyclo[3.1.0.02,4]hexane 8β,8'α-dimethyl-7α,7'β-bis(3-methoxy-4-hydroxyphenyl)cyclobutane 4,4'-((1R,2R,3S,4S)-3,4-dimethylcyclobutane-1,2-diyl)bis(methoxybenzene) caracasandiamide 3β,4β-bis(3',4'-dimethoxyphenyl)-1α-carboxy-2α-<butyl>cylobutanecarboxamide quinic acid diester of 3,4,3',4'-tetrahydroxy-β-truxinic acid 3,3′-difluoro-β-truxinic acid endiandrin B 3,3-Dimethyl-2,4-diphenyl-tricyclo[3.2.0.02,4]heptane (1R,6S,7S,8R)-7,8-Diphenyl-bicyclo[4.2.0]octane 1,5-Diphenyl-quadricyclan dimethyl t-3,t-4-di-(3,4,5-trimethoxyphenyl)cyclobutane-r-1,c-2-dicarboxylate (±)-(1R,5S,6R,7S)-6,7-bis(4-methoxyphenyl)-3-oxabicyclo[3.2.0]heptane 2-((1R,2S,3R,4R)-2-methyl-2-nitro-3,4-diphenylcyclobutyl)acetaldehyde 1α,2α-Di-(2-methoxy-phenyl)-cyclobutan-dicarbonsaeure-(3β,4β)-dimethylester o,o'-Dimethyl-β-truxillsaeuredimethylester 1,2-diisobutyryl-3,4-diphenyl-cyclobutane 3,4-bis(3,4-dimethylphenyl)cyclobutane-1,2-dicarboxylic acid (17S,18R,19S,20R)-18,19-bis(3,4-dimethylphenyl)-15,22-diazahexacyclo[21.2.2.211,14.12,6.017,20.010,30]triaconta-1(25),2,4,6(30),7,9,11(29),12,14(28),23,26-undecaene-16,21-dione 3,3-Dimethyl-2,4-diphenyl-endo-tricyclo<3.3.0.02,4>oct-6-en ((1S,2R,3S,4R)-3-Hydroxymethyl-1,4-diphenyl-bicyclo[2.2.0]hex-2-yl)-methanol (1R,7S,8R,11S)-8,11-Diphenyl-3,5-dioxa-4-thia-tricyclo[5.4.0.08,11]undecane 4,4-dioxide 4a,4b-Bis(4-methoxyphenyl)decahydrobiphenylene-1,8-dione 4a,4b-Bis(4-nitrophenyl)decahydrobiphenylene-1,8-dione 8-Methyl-4,4a-diphenyltetrahydro-1h,5h-3,4,4b-(methanetriyl)cyclopenta[1,3]cyclopropa[1,2-b]pyridin-2(3h)-one (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(4-tert-butyl-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester (S,S,S,S)-3,4-bis(2-diphenylphosphinylphenyl)-1,2-cyclobutanedimethyl di(diphenylphosphine) (1R,2R,3R,4R)-3,4-Bis-[2-(diphenyl-phosphinoyl)-phenyl]-cyclobutane-1,2-dicarboxylic acid diethyl ester (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(3,5-dimethyl-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester 4,4'-(3,4-diphenyl-cyclobutane-1,2-diyl)-bis-benzo[h]quinoline 4,4'-(3,4-diphenyl-cyclobutane-1,2-diyl)-bis-benzo[h]quinoline 3,4-diphenyl-3,4-dichlorocyclobutanodicarbox-1,2-dianilide (1S,5R,6R)-3-butyl-6,7-bis(2-hydroxyphenyl)-3-azabicyclo[3.2.0]heptane-2,4-dione (1R,2R,3R,4R)-3,4-Bis-{2-[bis-(4-methoxy-phenyl)-phosphinoyl]-phenyl}-cyclobutane-1,2-dicarboxylic acid diethyl ester 1,2-Diphenyl-1,2,2a,10b-tetrahydro-cyclobuta[l]phenanthrene all-cis-1,2-Dibenzyl-3,4-diphenylcyclobutan (3,4-diphenylcyclobutane-1,2-diyl)bis(phenylmethanone) 1,2-dibenzoyl-3,4-diphenyl-cyclobutane