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(1S,4R,5S)-4,7,7-Trimethyl-6-thia-1,5-bicyclo<3.2.1>octan-3-one

中文名称
——
中文别名
——
英文名称
(1S,4R,5S)-4,7,7-Trimethyl-6-thia-1,5-bicyclo<3.2.1>octan-3-one
英文别名
4,7,7-trimethyl-6-thia-1,5-bicyclo[3.2.1]octan-3-one;4,7,7-trimethyl-6-thiabicyclo[3.2.1]octan-3-one;(1S,4R,5S)-4,7,7-trimethyl-6-thiabicyclo[3.2.1]octan-3-one
(1S,4R,5S)-4,7,7-Trimethyl-6-thia-1,5-bicyclo<3.2.1>octan-3-one化学式
CAS
——
化学式
C10H16OS
mdl
——
分子量
184.302
InChiKey
ALOVQPMDMANUJI-FJXKBIBVSA-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):
    2
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    42.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    (R)-Carvone 在 ammonium sulfide 、 n-BuNBr 、 sulfur 作用下, 以 四氢呋喃 为溶剂, 反应 72.0h, 生成 (1S,4R,5S)-4,7,7-Trimethyl-6-thia-1,5-bicyclo<3.2.1>octan-3-one 、 (1S,4S,5S)-4,7,7-Trimethyl-6-thia-1,5-bicyclo<3.2.1>octan-3-one
    参考文献:
    名称:
    Synthesis and Evaluation of Enantiopure 6-Thiabicyclo[3.2.1]octanes for Asymmetric Epoxidation of Benzaldehyde
    摘要:
    报道了一种从香叶醇一步合成6-噻双环[3.2.1]辛烷-3-酮的方法。然后,在几步中进一步对手性硫化物进行了修饰,并将其用作有效的磺腈亚胺促进剂,促进醛的非对称环氧化。还描述了它们的香气特性。
    DOI:
    10.1055/s-2008-1077878
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文献信息

  • Phase-transfer-catalyzed reactions between polysulfide anions and .alpha.,.beta.-unsaturated carbonyl compounds
    作者:Eitan B. Krein、Zeev Aizenshtat
    DOI:10.1021/jo00074a043
    日期:1993.10
    Ammonium polysulfide reacts with alpha,beta-unsaturated ketones and aldehydes under PTC (phase transfer catalysis) conditions in a rather different manner than it does in homogeneous systems. 1,3-Diphenyl-2-propen-1-one (chalcone, 1) and 4-phenyl-3-buten-2-one (benzylideneacetone, 3) give sulfur-linked dimers (mainly disulfides). 3-Phenyl-2-propen-1-al (cinnamaldehyde) polymerizes. 1,5-Diphenyl-1,4-pentadien-3-one (dibenzylideneacetone, 7) gives the known six-membered ring thianones and new seven-membered ring 1,2-dithiepanones 9 along with a polymer. Carvone gives a disulfide dimer that converts to a mixture of bicyclic sulfur-containing compounds. Sodium polysulfide is much less effective because of the base-induced decomposition of either the products or the intermediates. Sodium sulfide reacts in the same manner as it does in homogenous systems.
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同类化合物

硫杂环庚烷-2-酮 硫杂环庚烷 环己硫醚 桉叶硫醚 四氢-6-硫代-1,4-乙桥-1H,3H-噻吩并(3,4-c)噻吩-3-酮 二氢-7-丁基-1,4-乙桥-1H,3H-噻吩并(3,4-c)噻吩-3,6(4H)-二酮 二氢-1,4-二甲基-1,4-乙桥-1H,3H-噻吩并(3,4-c)噻吩-3,6(4H)-二酮 二氢-1,4-乙基桥-1H,3H-噻吩并(3,4-c)噻吩-3,6(4H)-二酮 β.-D-半乳吡喃糖,1,6-二脱氧-1,6-环硫- 6-硫杂双环[3.2.1]辛烷 6-甲基-7-硫杂二环[4.1.0]庚烷 5-氧代噻吩-3-羧酸甲酯 5-氧代-4-噻吩甲酸乙酯 4,7,7-三甲基-6-硫代二环[3.2.1]辛烷 3-硫杂二环[3.2.1]辛烷-2-酮,1,8,8-三甲基-,(1R)- 3-甲基噻吩1,1-二氧化物 3-(4-甲基苯基)噻吩1,1-二氧化物 2-羟基噻烷 1-癸基2-[[1-(2-氯-5-磺基苯基)-4,5-二氢-3-甲基-5-羰基-1H-吡唑-4-基]偶氮]苯酸酯 1,6:4,5-二去氢-2,3-二脱氧-1-硫代己糖醇 (1S,4S,5S)-4,7,7-三甲基-6-硫代二环[3.2.4]辛烷 (-)-2,10-(3,3二氯樟脑)磺内酰胺 hexahydro-2,5-methano-thiopyrano[3,2-b]furan 4,4-dioxide (3aR,6R,6aR)-2,2-Dimethyl-4-(2-methyl-[1,3]dithian-2-yl)-6-(tetrahydro-pyran-2-yloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-ol trans-4,5-Dihydroxythiocane 3,4-dichloro-3-methyl-tetrahydro-thiophene 1,3-di-O-acetyl-2,5-anhydro-4-O-methyl-6-thio-α-D-glucoseptanose DL-(1,5/4)-4,7-O-benzylidene-5-C-hydroxymethyl-1,4-cyclohexanediol (1R,5S)-9-Thia-tricyclo[3.3.1.02,4]nonane 9,9-dioxide (1R,2R,5R,6S,9S,10S)-12-thiatetracyclo[8.3.0.02,5.06,9]tridecane Perhydro-bis-pyrano<2.3-b:3'.2'-e>-1,4-oxathian torilensulfat 2-acetoxy-1,5-dithiacyclooctane 1,2,4,6-Tetrakis-trifluoromethyl-3,5,7-trithia-tricyclo[4.1.0.02,4]heptane (2R,4R,6R)-4-Chloro-6-(1,2-dichloro-ethyl)-4-methyl-[1,2]oxathiane 2-oxide 2-[1,3,5]Trithian-2-yl-cyclohexanol trans-(RuCl2(S(CH2)3CH2)4) 4,6,7,7-tetramethyl-2-thia-bicyclo(2.2.2)oct-5-ene 2,2-dioxide (1R,5R)-9-Oxa-3,7-dithia-tricyclo[3.3.1.02,4]nonane 3,3,7,7-tetraoxide Dodecahydro-thianthren-tetroxyd {Rh2Cl2(μ-CO)(bis(ethylthio)methane)2} 2-(8β-hydroxy-1β-methyl-7β,2α,6α-tricyclo<5.4.0.02,6>undecyl)1,3-dithiane 17β-Hydroxymethyl-estra-4,8(14)-dien-3,3-ethylendithioketal (9'S,10'S,13'R,17'S)-17'-(4,4-dimethyl-3-methylenepentyl)-9',10',13'-trimethyl-1',2',6',7',9',10',11',12',13',15',16',17'-dodecahydrospiro[cyclopentane-1,3'-cyclopenta[a]phenanthrene] 1,2,3,4,5,6,7,8,8a,10a-Decahydro-9,10-dithiaphenanthren Acetic acid (3R,4S,5S,6R)-5-acetoxy-3,6-dimethoxy-thiepan-4-yl ester 3,4-Di-sec.-butoxysulfolan 1,8,15,22,29,36-hexathia-cyclodotetracontane (3aS,7aR)-3a,7a-Dimethyl-1,3,3a,4,7,7a-hexahydro-benzo[c]thiophene