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6-methoxy-4-phenyl-3,4-dihydro-2H-chromen-2-one | 40546-95-0

中文名称
——
中文别名
——
英文名称
6-methoxy-4-phenyl-3,4-dihydro-2H-chromen-2-one
英文别名
6-Methoxy-4-phenyl-3,4-dihydrocumarin;3,4-dihydro-6-methoxy-4-phenylcoumarin;3,4-dihydro-6-methoxy-4-phenyl-2H-1-benzopyran-2-one;6-methoxy-4-phenyl-chroman-2-one;6-Methoxy-4-phenyl-chroman-2-on;6-methoxy-4-phenyl-3,4-dihydrochromen-2-one
6-methoxy-4-phenyl-3,4-dihydro-2H-chromen-2-one化学式
CAS
40546-95-0
化学式
C16H14O3
mdl
——
分子量
254.285
InChiKey
LHFOVSGRSIATSD-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):
    3.1
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • Microwave accelerated the solvent-free synthesis of 4-aryl-3,4-dihydrocoumarin via the tandem reaction of cinnamic acids with phenols catalyzed by Amberlyst 15 resin
    作者:Huu-Phuoc Le、Cong-Thang Duong、Xuan-Triet Nguyen、Thi Xuan Thi Luu
    DOI:10.1080/00397911.2021.1925918
    日期:2021.7.18
    Abstract Amberlyst 15 resin supported the tandem reaction of cinnamic acids with phenols under solvent-free reaction condition has been introduced to afford 4-aryl-3,4-dihydrocoumarin (neoflavanone) derivatives. The efficiency of solid acidic sulfonic resin (A-15) has been illustrated in two reaction activation methods such as microwave irradiation and conventional heating. The important roles of Amberlyst
    摘要 Amberlyst 15 树脂支持肉桂酸与酚类在无溶剂反应条件下的串联反应,得到 4-芳基-3,4-二氢香豆素(新黄烷酮)衍生物。固体酸性磺酸树脂 (A-15) 的效率已通过微波辐射和常规加热两种反应活化方法进行了说明。Amberlyst 15 的重要作用通过在微波辐射的辅助下比常规加热在更短的时间内产生高产率 4-芳基-3,4-二氢香豆素,以及其六次催化剂运行的高回收率和可重复使用性而得到强烈强调。通过XRD和FE-SEM对原始催化剂和回收催化剂进行表征,以研究再利用催化剂的表面与其可回收性的相关性。
  • Selective Synthesis of 3,4-Dihydrocoumarins and Chalcones from Substituted Aryl Cinnamic Esters
    作者:Jae-Ho Jeon、Deok-Mo Yang、Jong-Gab Jun
    DOI:10.5012/bkcs.2011.32.1.65
    日期:2011.1.20
    Coumarins are ubiquitous in plant kingdom and have been used as antitumor, antifungals, anticoagulants, insecticides. Chalcones are also widespread in plant kingdom and have been known to possess diverse biological activities; antibacterial, antifungal, antitumor and anti-inflammatory, etc. As they are considered as important natural products, numerous synthetic approaches have been reported up to the present. We devise a new selective method of preparing dihydrocoumarins and chalcones from aryl cinnamates by the selection of reagents. Dihydrocoumarin derivatives were prepared selectively by using intramolecular cyclization catalyzed by p-toluene sulfonic acid. Also, chalcones were prepared by Fries-rearrangement catalyzed by $TiCl_4$. This method can be used for preparing various coumarin & chalcone compounds.
    香豆素广泛存在于植物王国中,并已被用作抗癌剂、抗真菌剂、抗凝血剂和杀虫剂。查尔酮也在植物王国中广泛分布,并且已知具有多种生物活性,包括抗菌、抗真菌、抗癌和抗炎等。由于它们被认为是重要的天然产物,迄今为止已经报道了许多合成方法。我们设计了一种新的选择性方法,通过选择试剂,从芳基肉桂酸制备二氢香豆素和查尔酮。通过使用对甲苯磺酸催化的分子内环化反应,选择性地制备了二氢香豆素衍生物。此外,还通过三氯化钛催化的Fries重排反应制备了查尔酮。这种方法可以用于制备各种香豆素和查尔酮化合物。
  • CuSCN Catalyzed Conjugate Addition of Grignard Reagents to Substituted Coumarins with Dilithium Tetrachloromanganate
    作者:Mohan B. Kale、Shrikant B. Jagtap、Santosh S. Devkate
    DOI:10.14233/ajchem.2020.22701
    日期:——

    The regioselective 1,4-addition of CuSCN catalyzed Grignard reagents to the substituted coumarins are reported. The Li2MnCl4 reagent is used to transmetallate magnesium by manganese. It adds regioselectively to coumarins and forms 1,4-addition products with higher yield under the atmosphere of nitrogen gas and at a lower temperature

    报道了CuSCN催化的Grignard试剂对取代香豆素的区域选择性1,4-加成。使用Li2MnCl4试剂通过锰来进行金属转移与镁。在氮气气氛下且在较低温度下,它对香豆素进行区域选择性加成,并形成产率更高的1,4-加成产物。
  • Microwave-Assisted One-Pot Synthesis of Dihydrocoumarins from Phenols and Cinnamoyl Chloride
    作者:Yuan Ma、Zhen Zhang、Yufen Zhao
    DOI:10.1055/s-2008-1042921
    日期:——
    A facile approach has been developed for the synthesis of dihydrocoumarin derivatives through the reaction of phenols and cinnamoyl chloride in the presence of ecofriendly solid-acid catalyst montmorillonite K-10 via a tandem esterification-Friedel-Crafts alkylation process under microwave irradiation. The catalyst could be easily recovered and recycled.
    通过微波辐照下的串联酯化-Friedel-Crafts 烷基化过程,在生态友好型固体酸催化剂蒙脱石 K-10 的存在下,通过苯酚和肉桂酰氯的反应合成二氢香豆素衍生物,开发了一种简便的方法。催化剂易于回收和循环使用。
  • TMSOTf-catalyzed intramolecular seleno-arylation of tethered alkenes: A novel method for the solid-phase synthesis of dihydrocoumarins and coumarins
    作者:E Tang、Wen Li、Zhang Yong Gao、Xi Gu
    DOI:10.1016/j.cclet.2012.03.022
    日期:2012.6
    TMSOTf-catalyzed intramolecular seleno-arylation of tethered alkenes was performed using polystyrene-supported succinimidyl selenide as the selenium source. This catalytic process provides an efficient method for the regioselective synthesis of dihydrocoumarins possessing a seleno-functionality, followed by traceless cleavage of selenium linker to provide dihydrocoumarins and coumarins in good yields and purities. (C) 2012 E Tang. Published by Elsevier B.V on behalf of Chinese Chemical Society. All rights reserved.
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同类化合物

黄檀色烯 黄檀素 铁力木苦素 贝伐他汀 红厚壳内酯 头孢克肟侧链酸活性酯 外消旋6-甲氧羰基-4-苯基-3,4-二氢香豆素 外消旋-6-甲基-4-苯基-2-色满醇 塞曲司特 四甲基罗丹明-5-马来酰亚胺 乙酮,1-[8-(4-羟基-3,5-二甲氧苯基)-6-甲基-8H-1,3-二噁唑并[4,5-g][1]苯并吡喃-7-基]- N,N-二乙基-4-(5-羟基螺[2H-1-苯并吡喃-2,4'-哌啶]-4-基)苯甲酰胺盐酸盐 L-苯丙氨酸,N-[(7-羟基-2-羰基-4-苯基-2H-1-苯并吡喃-8-基)甲基]- Atto590NHS酯 8-羟基-4-苯基-2-3,4-二氢苯并吡喃酮 8-乙酰基-5,7-二羟基-4-苯基色烯-2-酮 8-(4-甲氧苯基)-6-甲基-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯-6-醇 8-(2-羟基-3-甲氧苯基)-7-甲基-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯-6-醇 8-(2-甲氧苯基)-6,7-二甲基-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯-6-醇 8-(2,4-二甲氧基苯基)-6-甲氧基-6,7-二甲基-7,8-二氢吡喃并[6,5-f][1,3]苯并二氧戊环 7-羟基-8-甲基-4-苯基-2H-色烯-2-酮 7-羟基-6-戊基-4-苯基色烯-2-酮 7-羟基-4-苯基香豆素 7-羟基-4-苯基-3-(4-羟基苯基)香豆素 7-羟基-4-苯基-3-(3-吡啶基)-2H-1-苯并吡喃-2-酮 7-羟基-4-(4-甲氧基苯基)-3,4-二氢-2H-1-苯并吡喃-2-酮 7-羟基-4-(3-三氟甲基苯基)香豆素 7-羟基-3-甲基-4-苯基香豆素 7-羟基-3-(4-甲氧苯基)-4-苯基-2H-色烯-2-酮 7-甲氧基-8-甲基-4-苯基色烯-2-酮 7-甲氧基-4-苯基色烯-2-酮 7-甲氧基-3-甲基-4-苯基-2H-色烯-2-酮 7-甲基-4-苯基-3,4-二氢色烯-2-酮 7-溴-4-(3-甲基苯基)-2H-色烯-2-酮 7-乙酰氧基-4-苯基-色烯-2-酮 7-乙氧基-4-苯基-2H-色烯-2-酮 7-[4-(1-乙基-1-羟基-丙基)-[1,2,3]三唑-1-基甲基]-4-(3-氟-苯基)-色烯-2-酮 7-(溴甲基)-4-(3-氟苯基)-2H-色烯-2-酮 7-(叠氮甲基)-4-(3-甲基苯基)-2H-色烯-2-酮 7-(叠氮甲基)-4-(3-氟苯基)-2H-色烯-2-酮 7,8-二羟基-4-苯基香豆素 7,8-二乙酰氧基-4-苯基香豆素 6-羧基-4-苯基-3,4-二氢香豆素 6-羟基-4-苯基-3,4-二氢色烯-2-酮 6-甲氧基-7-甲基-8-(3,4,5-三甲氧苯基)-7,8-二氢-6H-[1,3]二噁唑并[4,5-g]色烯 6-甲基-6-吡咯烷-1-基-8-(3,4,5-三甲氧基苯基)-7,8-二氢吡喃并[6,5-f][1,3]苯并二氧戊环-7-羧酸乙酯 6-甲基-4-苯基香豆素 6-甲基-4-苯基色满-2-酮 6-甲基-4-(4-甲基苯基)-3-苯基色烯-2-酮 6-溴-3,4-二氢-4-苯基-2H-1-苯并吡喃-2-酮