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cis(3a,7a)-3-acetyl-2-methyl-3a,5,6,7a-tetrahydro-4H-furo<2,3-b>pyran | 82469-41-8

中文名称
——
中文别名
——
英文名称
cis(3a,7a)-3-acetyl-2-methyl-3a,5,6,7a-tetrahydro-4H-furo<2,3-b>pyran
英文别名
cis-(3a,7a)-3-Acetyl-2-methyl-3a,5,6,7a-tetrahydro-4H-furo[2,3-b]pyran;cis-2-methyl-3-acetyl-1,8-dioxabicyclo<4.3.0>non-2-ene;cis-2-methyl-3-acetyl-1,8-dioxabicyclo[4.3.0]non-2-ene;1-[(3aS,7aR)-2-methyl-4,5,6,7a-tetrahydro-3aH-furo[2,3-b]pyran-3-yl]ethanone
cis(3a,7a)-3-acetyl-2-methyl-3a,5,6,7a-tetrahydro-4H-furo<2,3-b>pyran化学式
CAS
82469-41-8
化学式
C10H14O3
mdl
——
分子量
182.219
InChiKey
QWKODDUVGOKSPA-WCBMZHEXSA-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):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    3,4-二氢-2H-吡喃(2Z)-3-偶氮基-4-氧代-2-戊烯-2-醇六氟乙酰丙酮化铜的水合物 作用下, 以 氟苯 为溶剂, 以72%的产率得到cis(3a,7a)-3-acetyl-2-methyl-3a,5,6,7a-tetrahydro-4H-furo<2,3-b>pyran
    参考文献:
    名称:
    Studies on the origin of dihydrofurans from .alpha.-diazocarbonyl compounds. Concerted 1,3-dipolar cycloaddition vs. nonsynchronous coupling in the copper chelate catalyzed reactions of .alpha.-diazodicarbonyl compounds with electron-rich olefins
    摘要:
    DOI:
    10.1021/jo00140a030
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文献信息

  • Synthesis of fused acetal derivatives by manganic acetate promoted additions to endocyclic enol ethers
    作者:John M. Mellor、Shahid Mohammed
    DOI:10.1016/s0040-4020(01)87230-6
    日期:1993.8
    Reaction of manganic acetate in acetic acid with β-diketones and β-ketoesters leads to generation of intermediates, which add efficiently to endocyclic unsaturated enol ethers to afford fused acetals.
    乙酸锰在乙酸中与β-二酮和β-酮​​酸酯的反应导致生成中间体,该中间体可有效地添加到环内不饱和烯醇醚中以提供稠合缩醛。
  • Tetrabutylammonium Peroxydisulfate in Organic Synthesis; IX: A Convenient Approach to the Synthesis of Fused Acetal Derivatives by Tetrabutylammonium Peroxydisulfate-Mediated Oxidative Cycloaddition of 1,3-Dicarbonyl Compounds to Cyclic Enol Ethers
    作者:Fen-Er Chen、Han Fu、Ge Meng、Yu Cheng、Ye-Li Hu
    DOI:10.1055/s-2000-6312
    日期:——
    A number of fused acetal derivatives were prepared in 82-90% yield by tetrabutylammonium peroxydisulfate-mediated oxidative cycloaddition of 1,3-diketones or 1,3-diketoesters to cyclic enol ethers in the presence of a base such as potassium acetate in acetonitrile.
    通过四丁基过氧化二硫酸铵介导的 1,3-二酮或 1,3-二酮酯与环状烯醇醚在乙腈中的氧化环化反应,制备出了一些融合缩醛衍生物,收率为 82-90%。
  • Synthesis of fused acetals by ceric ammonium nitrate mediated cycloaddition of 1,3-dicarbonyl compounds to cyclic enol ethers
    作者:Subhas Chandra Roy、Pijus Kumar Mandal
    DOI:10.1016/0040-4020(96)00728-4
    日期:1996.9
    Treatment of β-diketones and β-ketoesters with ceric ammonium nitrate and sodium hydrogen carbonate in acetonitrile leads to the formation of intermediates which add efficiently to cyclic enol ethers to furnish fused acetals in good yields.
    用硝酸铈铵和碳酸氢钠在乙腈中处理β-二酮和β-酮​​酸酯会导致形成中间体,该中间体可有效地添加到环状烯醇醚中,从而以高收率提供熔融缩醛。
  • Studies on the origin of dihydrofurans from .alpha.-diazocarbonyl compounds. Concerted 1,3-dipolar cycloaddition vs. nonsynchronous coupling in the copper chelate catalyzed reactions of .alpha.-diazodicarbonyl compounds with electron-rich olefins
    作者:Miguel E. Alonso、Angelina Morales、A. Wladimir Chitty
    DOI:10.1021/jo00140a030
    日期:1982.9
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同类化合物

马桑宁内酯 苦毒浆果[木防已属] 苦亭 艾瑞布林中间体 艾瑞布林 甲磺酸艾日布林 木防己苦毒宁 全内酯 二氢苦毒宁 6-甲基-4-氧代-4H-呋喃并[3,2-c]吡喃-3-甲酰氯 6-(4-羟基苯基)-2,3,3-三甲基-2H-呋喃并[5,4-b]吡喃-4-酮 4H-呋喃并[2,3-c]吡喃基莫匹罗星钠 3-甲基2H-呋喃并[2,3-c]吡喃-2-酮 3,5-二甲基2H-呋喃并[2,3-c]吡喃-2-酮 2H-呋喃并[2,3-c]吡喃-2-酮 2-[(1E,3E)-己-1,3-二烯基]-2,6-二甲基-5,6-二氢呋喃并[5,4-b]吡喃-3,4-二酮 (3aS,5S,6R,9E,14R,15R,15aR)-2,3,3a,4,5,6,7,8,11,12,13,14,15,15alpha-十四氢-6,10,14-三甲基-3-亚甲基-2-氧代-5,15-环氧环十四烷并[b]呋喃-6-醇乙酸酯 (3aR,4S,7aR)-4-羟基-3,3a,4,7a-四氢呋喃并[5,4-b]吡喃-2-酮 5-hydroxymethyl-3-methyl-2H-furo[2,3-c]pyran-2-one 5-fluoromethyl-2H-furo[2,3-c]pyran-2-one 5-chloromethyl-2H-furo[2,3-c]pyran-2-one 10,11-Anhydro-5-deoxy-1,2-O-isopropylidene-9-O-(methoxymethyl)-β-L-xylo-L-ido-7-undeculofuranose-(1,4)-pyranose-(7,3) 3,7-dimethyl-2H-furo[2,3-c]pyran-2-one 4R-(3αβ,3aβ,4β,5α,6β,7aβ)hexahydro-2,2-dimethyl-4,5-bis(phenylmethoxy)-6-[(phenylmethoxy)methyl]4H-furo[2,3-b]pyran-3-ol 10,10-dimethyl-5-(methylsulfanyl)-10,11-dihydro-8H-pyrano[4',3':4,5]furo[3,2-e]tetrazolo[1,5-c]pyrimidine (R)-3-((2R,3R,5aR,7R,9aS)-3-hydroxyhexahydro-2H-2,5a-methanopyrano[3,2-e][1,4]dioxepin-7-yl)-2-methylpropanenitrile 13-methyl-8,10,12-trioxapentacyclo[5.5.2.02,6.O3,11.05,9]-13-tetradecene 2,3,4,4a,7,8-Hexahydro-6H-2-(acetoxymethyl)-3,4-diacetoxy-1,9-dioxacyclohexainden-5-one 2,3,4,4a,7,8-Hexahydro-6H-2-methoxy-1,9-dioxacyclohexainden-5-one (-)-3a-methyl-3a,4-dihydro-1H,3H-furo[3,4-c]pyran-6,6,7-tricarboxylic acid 6,6-diethyl ester 7-methyl ester (+)-8-epi-altholactone 4-(perfluorophenyl)-3-phenylhexahydro-1H-furo[3,4-c]pyran [(2R,11S,12R,14R,15R,17R,19S)-19-tert-butyldiphenylsiloxymethyl-15-methyl-13,18-dioxadispiro(2H-3,6-dihydropyran-6,5'-oxolane-2',3''-bicyclo[4.3.0]nonane)-2-yl]phenylmethoxymethane (3aS,5S,9bS)-5-methyl-3,3a-dihydro-5H-furo[3,2-c]isochromene-2,6,9-(9bH)-trione (3aR,5R,7aR)-5-(2-hydroxypropan-2-yl)-7a-methylhexahydro-2H-furo[3,2-b]pyran-2-one 2,2,3b-trimethyl-7-vinyl-3a,5,7a,8a-tetrahydro-3bH-1,3,4,8-tetracyclopenta[a]indene ethyl 4-oxo-3-phenyl-3,3a,4,6-tetrahydro-1H-furo[3,4-c]pyran-3a-carboxylate methyl (2R,2aR,4aS,7aS,7bS)-2-methoxy-6-methyl-4-oxo-5-pentyl-2a,4,4a,7b-tetrahydro-2H-1,3,7-trioxacyclopenta[cd]indene-7a-carboxylate 4-nonyl-3-phenylhexahydro-1H-furo[3,4-c]pyran 3'-(4-methoxyphenyl)-7a'-methyl-4'H,6'H-spiro[cyclohexane-1,5'-furo[2,3-b]pyran]-2'(7a'H)-one 3',7a'-dimethyl-4'H,6'H-spiro[cyclohexane-1,5'-furo[2,3-b]pyran]-2'(7a'H)-one 2-(methylsulfanyl)-5,6-dihydro-4H-furo[2,3-b]pyran 1,1-(3-dimethylamino-3-phenylpentamethylen)-3,4-dihydro-1H-2,9-dioxafluoren 7-cyclopropyl-4,5,7,7a-tetrahydro-furo[2,3-c]pyran-2-one 7-cyclopropyl-3-phenyl-4,5,7,7a-tetrahydro-furo[2,3-c]pyran-2-one 7-cyclopropyl-3-phenyl-4,5,7,7a-tetrahydro-furo[2,3-c]pyran-2-one (4'R)-6-O-(4-cyanophenyl)-1,2,3,4-tetradeoxy-4'-(2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,9-heptadecafluorononyl)-2',3',4',5'-tetrahydro-α-D-erythro-hexopyranoso[1,2-b]furan 2,2,3,6-tetramethyl-2,3-dihydro-4H-furo[2,3-b]pyran-4-one (1aR,4aS,5R)-7-carboethoxy-5-methylethyl-tetrahydrofurano[2,3-b]3,4-dihydro-2H-pyran (3aS,4S,7aR)-ethyl 4-methyl-3,3a,4,7a-tetrahydro-2H-furo[2,3-b]pyran-6-carboxylate