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syn-(1α,2β,3β,4β)-1,2-bis(4-methoxyphenyl)-3,4-dimethylcyclobutane | 19043-23-3

中文名称
——
中文别名
——
英文名称
syn-(1α,2β,3β,4β)-1,2-bis(4-methoxyphenyl)-3,4-dimethylcyclobutane
英文别名
(1α,2α,3β,4β)-1,2-bis(4-methoxyphenyl)-3,4-dimethylcyclobutane;1ref-2cis-Bis-(p-anisyl)-3trans-4trans-dimethyl-cyclobutan;1-methoxy-4-[(1S,2R,3S,4R)-2-(4-methoxyphenyl)-3,4-dimethylcyclobutyl]benzene
syn-(1α,2β,3β,4β)-1,2-bis(4-methoxyphenyl)-3,4-dimethylcyclobutane化学式
CAS
19043-23-3
化学式
C20H24O2
mdl
——
分子量
296.409
InChiKey
FRCHSWTWZRVQDF-YKLJGAPNSA-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:
    400.3±45.0 °C(Predicted)
  • 密度:
    1.031±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    syn-(1α,2β,3β,4β)-1,2-bis(4-methoxyphenyl)-3,4-dimethylcyclobutane 在 tris-(4-bromophenyl)aminium hexachloroantimonate 作用下, 以 二氯甲烷 为溶剂, 生成 茴香烯
    参考文献:
    名称:
    Cation radical catalyzed olefin cyclodimerization
    摘要:
    DOI:
    10.1021/ja00341a060
  • 作为产物:
    参考文献:
    名称:
    反式茴香脑的光化学反应
    摘要:
    已经通过化学方法获得了新型的反式茴香脑二聚体。二聚化以严格的立体特异性进行,并且已经确定二聚体的结构为1,顺式-2-二-对-茴香基-反式-3,反式-4-二甲基环丁烷。将二聚体转化成相应的二酚,二乙酸酯和1,顺式-2-二甲基-反式-3,反式-4-二苯基环丁烷。烃是通过还原从β-精氨酸独立获得的。由肉桂酸二聚体类似地制备了一些二甲基二苯基环丁烷异构体,并比较了NMR光谱。
    DOI:
    10.1016/0040-4020(68)88120-7
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文献信息

  • [2+2]-Cycloaddition Reaction of Styrene Derivatives Using an Fe(III) Salt Catalyst
    作者:Hiroyuki Ohara、Toshiyuki Itoh、Masaharu Nakamura、Eiichi Nakamura
    DOI:10.1246/cl.2001.624
    日期:2001.7
    Iron(III) perchlorate catalyzed cyclodimerization of trans-anethole gave trans,anti,trans-cyclobutane stereospecifically in good yield. Alumina supported iron(III) perchlorate was an especially efficient one-electron oxidation reagent.
    高氯酸铁 (III) 催化的反式茴香脑环二聚反应以良好的收率立体定向地得到反式、反式、反式环丁烷。氧化铝负载的高氯酸铁 (III) 是一种特别有效的单电子氧化试剂。
  • 9,10-Dicyanoanthracene-sensitized photo-oxygenation of trans-1,2-di-(carbazol-9-yl)cyclobutane via electron-transfer
    作者:Kazuhiko Mizuno、Kazuhiro Murakami、Nobuhiro Kamiyama、Yoshio Otsuji
    DOI:10.1039/c39830000462
    日期:——
    9,10-Dicyanoanthracene-sensitized photo-oxygenation of trans-1,2-di(carbazol-9-yl)cyclobutane in acetonitrile efficiently affords 3,6-di(carbazol-9-yl)-1,2-dioxan.
    在乙腈中对反式-1,2-二(咔唑-9-基)环丁烷进行9,10-二氰基蒽敏感的光氧合可有效提供3,6-二(咔唑-9-基)-1,2-二恶烷。
  • Anethole Isomerization and Dimerization Induced by Acid Sites or UV Irradiation
    作者:Hans T. Castro、Jairo René Martínez、Elena Stashenko
    DOI:10.3390/molecules15075012
    日期:——
    The formation of cis-anethole and various dimers as a result of the exposure of trans-anethole to microporous solid acids (dealuminated HY zeolites), or UV-Vis irradiation was established by means of high resolution gas chromatography coupled to mass spectrometry. 3,4-bis-(4-Methoxyphenyl)-(E)-hex-2-ene was the most abundant compound among eight different methoxyphenyl-disubstituted hexenes produced
    由于反式茴香脑暴露于微孔固体酸(脱铝 HY 沸石)或 UV-Vis 照射,顺式茴香脑和各种二聚体的形成是通过高分辨率气相色谱与质谱联用建立的。3,4-双-(4-甲氧基苯基)-(E)-己-2-烯是由HY沸石诱导的亲电加成和消除反应产生的八种不同甲氧基苯基二取代己烯中含量最高的化合物。(1a,2a,3b,4b)-1,2-双(4-甲氧基苯基)-3,4-二甲基环丁烷是发现的 5 种甲氧基苯基-二取代环丁烷和顺式茴香脑的混合物中的主要成分,经过 UV-甲苯中的反式茴香脑溶液的可见光照射。
  • Electron-transfer-induced photoisomerization, dimerization, and oxygenation of trans- and cis-anethole. The role of monomer and dimer cation radicals
    作者:Frederick D. Lewis、Masanobu. Kojima
    DOI:10.1021/ja00234a014
    日期:1988.12
  • Acyclic 1,4-radical cations. Direct observation and stability
    作者:Sachiko Tojo、Susumu Toki、Setsuo Takamuku
    DOI:10.1021/jo00021a054
    日期:1991.10
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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