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1-(2-甲基丙-1-烯基)吡咯烷-2-酮 | 6908-66-3

中文名称
1-(2-甲基丙-1-烯基)吡咯烷-2-酮
中文别名
——
英文名称
N-(2-methyl-1-propenyl)-2-pyrrolidinone
英文别名
1-(2-Methyl-1-propenyl)pyrrolidone;1-(2-methylprop-1-enyl)pyrrolidin-2-one
1-(2-甲基丙-1-烯基)吡咯烷-2-酮化学式
CAS
6908-66-3
化学式
C8H13NO
mdl
——
分子量
139.197
InChiKey
FMMKZWYWJFOKQU-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

物化性质

  • 沸点:
    115-115.2 °C(Press: 10 Torr)
  • 密度:
    1.083±0.06 g/cm3(Predicted)
  • 保留指数:
    1260

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:d8ed87e174b9e3385c4ba50f841097a7
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反应信息

  • 作为反应物:
    描述:
    1-(2-甲基丙-1-烯基)吡咯烷-2-酮氧气一水合肼7-(trifluoromethyl)-1,10-ethyleneisoalloxazinium chloride 作用下, 以 为溶剂, 100.0 ℃ 、101.33 kPa 条件下, 反应 18.0h, 生成 1-(2-甲基丙基)吡咯烷-2-酮
    参考文献:
    名称:
    水中酰胺的有机催化二酰亚胺还原。
    摘要:
    桥接的黄酮有机催化剂在二酰亚胺介导的水性条件下的酰胺还原中显示出功效。这代表了富电子烯烃的第一次二酰亚胺还原,并为使用烷基化剂进行N-烷基化提供了一种清洁的替代方法。
    DOI:
    10.1039/c0cc02272a
  • 作为产物:
    描述:
    2-吡咯烷酮1-溴-2-甲基-1-丙烯copper(l) iodideN,N-二甲基甘氨酸盐酸盐caesium carbonate 作用下, 以 1,4-二氧六环 为溶剂, 反应 24.0h, 以62%的产率得到1-(2-甲基丙-1-烯基)吡咯烷-2-酮
    参考文献:
    名称:
    CuI/N,N-Dimethylglycine-Catalyzed Coupling of Vinyl Halides with Amides or Carbamates
    摘要:
    The Cul-catalyzed coupling reaction of vinyl halides with amides or carbamates proceeds well at room temperature to 80 degreesC in dioxane to give enamides using NN-dimethylglycine as the promoter and Cs2CO3 as the base. The geometry of the C-C double bond is retained during the reaction course.
    DOI:
    10.1021/ol049464i
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文献信息

  • Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds
    申请人:——
    公开号:US20030065187A1
    公开(公告)日:2003-04-03
    The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.
    本发明涉及铜催化的碳-杂原子和碳-碳键形成方法。在某些实施例中,本发明涉及铜催化的方法,用于在酰胺或胺基团的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在其他实施例中,本发明涉及铜催化的方法,用于在酰基肼的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在另一些实施例中,本发明涉及铜催化的方法,用于在含氮杂环芳烃(例如吲哚、吡唑和吲哌)的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在某些实施例中,本发明涉及铜催化的方法,用于在醇的氧原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氧键。本发明还涉及铜催化的方法,用于在包含亲核碳原子的反应物(例如烯醇酸盐或丙二酸盐负离子)与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-碳键。重要的是,由于催化剂中铜的低成本,本发明的所有方法都相对廉价。
  • Regioselective Hydrothiolation of Alkenes Bearing Heteroatoms with Thiols Catalyzed by Palladium Diacetate
    作者:Taichi Tamai、Akiya Ogawa
    DOI:10.1021/jo500586a
    日期:2014.6.6
    examples of transition-metal-catalyzed hydrothiolation of alkynes, the corresponding catalytic addition of thiols to alkenes has remained undeveloped. However, a novel Pd-catalyzed addition of thiols to alkenes bearing a heteroatom, such as oxygen and nitrogen, is found to proceed under mild conditions to give the corresponding Markovnikov adducts, regioselectively, in good yields.
    与过渡金属催化的炔烃氢硫醇化反应的许多实例形成鲜明对比的是,尚未开发出相应的硫醇向烯烃的催化加成反应。然而,发现在温和的条件下,新型的钯催化的硫醇向带有杂原子的烯烃(如氧和氮)进行新型的Pd催化加成反应,可以区域选择性地以高收率得到相应的马尔可夫尼科夫加合物。
  • CATALYSTS FOR EFFICIENT Z-SELECTIVE METATHESIS
    申请人:Trustees of Boston College
    公开号:US20140371454A1
    公开(公告)日:2014-12-18
    The present application provides, among other things, compounds and methods for metathesis reactions. In some embodiments, provided compounds promote highly efficient and highly Z-selective metathesis. In some embodiments, provided compounds and methods are particularly useful for producing allyl alcohols. In some embodiments, provided compounds have the structure of formula I. In some embodiments, provided compounds comprise ruthenium, and a ligand bonded to ruthenium through a sulfur atom.
    本申请提供了化合物和用于交换反应的方法,其中所提供的化合物在某些实施方式中促进高效和高度Z-选择性的交换反应。在某些实施方式中,所提供的化合物和方法特别适用于生产烯丙醇。在某些实施方式中,所提供的化合物具有式I的结构。在某些实施方式中,所提供的化合物包含钌,并且与钌通过硫原子结合的配体。
  • Re(I)-catalyzed hydropropargylation of enamides: a useful method for the preparation of 4-pentynylamine derivatives
    作者:Shoya Watanabe、Akane Ario、Nobuharu Iwasawa
    DOI:10.1038/s41429-019-0162-3
    日期:2019.6
    complex intermediate, followed by intramolecular hydrogen transfer to the iminium carbon. This method is useful for the synthesis of 4-pentynylamine derivatives from enamides and easily available propargyl ether. Moreover, tandem cyclization reaction was achieved to afford a pyrrolidine derivative in a single operation by using a secondary enamide.
    通过将酰胺的1,4-加成到α,β-不饱和卡宾配合物中间体上,然后将分子内的氢转移到亚胺碳上,可以以高收率实现酰胺的加氢炔丙基化。该方法可用于由酰胺和容易获得的炔丙基醚合成4-戊炔胺衍生物。此外,通过使用仲烯酰胺在一次操作中实现串联环化反应以提供吡咯烷衍生物。
  • Copper-catalyzed formation of carbon heteroatom and carbon-carbon bonds
    申请人:Buchwald L. Stephen
    公开号:US20050215794A1
    公开(公告)日:2005-09-29
    The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.
    本发明涉及铜催化的碳-杂原子和碳-碳键形成方法。在某些实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和酰胺或胺基团的氮原子之间形成碳-氮键。在其他实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和酰肼的氮原子之间形成碳-氮键。在其他实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和含氮杂环芳香族化合物(例如吲哚、吡唑和吲唑)的氮原子之间形成碳-氮键。在某些实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和醇的氧原子之间形成碳-氧键。本发明还涉及铜催化的方法,用于在包含亲核碳原子(例如烯醇酸根离子或马隆酸根离子)的反应物和苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳之间形成碳-碳键。重要的是,由于催化剂中铜的低成本,本发明的所有方法都相对廉价易行。
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同类化合物

(2R,2''R)-(-)-2,2''-联吡咯烷 麦角甾-7,22-二烯-3-基亚油酸酯 马来酰亚胺霉素 马来酰亚胺基甲基-3-马来酰亚胺基丙酸酯 马来酰亚胺丙酰基-dPEG4-NHS 马来酰亚胺-酰胺-PEG6-琥珀酰亚胺酯 马来酰亚胺-酰胺-PEG24-丙酸 马来酰亚胺-酰胺-PEG12-丙酸 马来酰亚胺-四聚乙二醇-羧酸 马来酰亚胺-四聚乙二醇-丙酸叔丁酯 马来酰亚胺-六聚乙二醇-丙酸叔丁酯 马来酰亚胺-二聚乙二醇-丙酸叔丁酯 马来酰亚胺-三(乙烯乙二醇)-丙酸 马来酰亚胺-一聚乙二醇-羧酸 马来酰亚胺-一聚乙二醇-丙烯酸琥珀酰亚胺酯 马来酰亚胺-PEG3-羟基 马来酰亚胺-PEG2-胺三氟醋酸盐 马来酰亚胺-PEG2-琥珀酰亚胺酯 马来酰亚胺 频哪醇硼酸酯 顺式4-甲基吡咯烷酮-3-醇盐酸盐 顺式3,4-二氨基吡咯烷-1-羧酸叔丁酯 顺式-二甲基 1-苄基吡咯烷-3,4-二羧酸 顺式-N-[2-(2,6-二甲基-1-哌啶基)乙基]-2-氧代-4-苯基-1-吡咯烷乙酰胺 顺式-N-Boc-吡咯烷-3,4-二羧酸 顺式-5-苄基-2-叔丁氧羰基六氢吡咯并[3,4-c]吡咯 顺式-4-氧代-六氢-吡咯并[3,4-C]吡咯-2-甲酸叔丁酯 顺式-3-氟-4-羟基吡咯烷-1-羧酸叔丁酯 顺式-3-氟-4-甲基吡咯烷盐酸盐 顺式-2-甲基六氢吡咯并[3,4-c]吡咯 顺式-2,5-二甲基吡咯烷 顺式-1-苄基-3,4-吡咯烷二甲酸二乙酯 顺式-(9CI)-3,4-二乙烯-1-(三氟乙酰基)-吡咯烷 顺-八氢环戊[c]吡咯-5-酮盐酸盐 非星匹宁 阿维巴坦中间体1 阿曲生坦中间体 阿曲生坦 间甲氧基苯乙腈 铂(2+)羟基乙酸酯-吡咯烷-3-胺(1:1:1) 钾2-氧代吡咯烷-1-磺酸酯 钠1-[(9E)-9-十八碳烯酰基氧基]-2,5-二氧代-3-吡咯烷磺酸酯 金刚烷-1-基(吡咯烷-1-基)甲酮 酸-1-吡咯烷-1,4-氨基-2-甲基-1,1,1-二甲基乙基酯,(2S,4R)- 酚丙氢吡咯 试剂3-Mercaptopropanyl-N-hydroxysuccinimideester 西他利酮 血红素酸 螺虫乙酯残留代谢物Mono-Hydroxy 萘吡坦