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(4S,5S)-4-p-tolylthio-5-trifluoromethyldihydrofuran-2-one | 473435-95-9

中文名称
——
中文别名
——
英文名称
(4S,5S)-4-p-tolylthio-5-trifluoromethyldihydrofuran-2-one
英文别名
(4S,5S)-4-(4-methylphenyl)sulfanyl-5-(trifluoromethyl)oxolan-2-one
(4S,5S)-4-p-tolylthio-5-trifluoromethyldihydrofuran-2-one化学式
CAS
473435-95-9
化学式
C12H11F3O2S
mdl
——
分子量
276.279
InChiKey
WQKKYWCEVHFPEL-GXSJLCMTSA-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):
    3.6
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    51.6
  • 氢给体数:
    0
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (4S,5S)-4-p-tolylthio-5-trifluoromethyldihydrofuran-2-one 氢气 作用下, 以 乙二醇 为溶剂, 反应 2.0h, 以62%的产率得到(-)-(R)-5-三氟甲基二氢呋喃-2-酮
    参考文献:
    名称:
    Stereoselective Synthesis of Both Enantiomers of Trifluoro-γ-valerolactone and Pentafluoro-γ-caprolactone
    摘要:
    Both enantiomers of 5-(trifluoromethyl)dihydrofuran-2-one (1a) and 5-(pentafluoroethyl)dihydrofuran-2-one (1b) have been synthesised stereoselectively, in four steps, starting from chiral (R)- or (S)-3-[(4-methylphenyl)sulfinyl]propionic acid (2) and commercially available perfluorinated esters. Compound (+)-(S)-1b is the pentafluoro analogue of the aggregation pheromone of Trogoderma glabrum.
    DOI:
    10.1002/1099-0690(200206)2002:12<1895::aid-ejoc1895>3.0.co;2-1
  • 作为产物:
    描述:
    (3S,4S)-5,5,5-trifluoro-4-hydroxy-3-(p-tolylthio)pentanoic acid溶剂黄146 作用下, 以 甲苯 为溶剂, 反应 4.0h, 以73.2%的产率得到(4S,5S)-4-p-tolylthio-5-trifluoromethyldihydrofuran-2-one
    参考文献:
    名称:
    Stereoselective Synthesis of Both Enantiomers of Trifluoro-γ-valerolactone and Pentafluoro-γ-caprolactone
    摘要:
    Both enantiomers of 5-(trifluoromethyl)dihydrofuran-2-one (1a) and 5-(pentafluoroethyl)dihydrofuran-2-one (1b) have been synthesised stereoselectively, in four steps, starting from chiral (R)- or (S)-3-[(4-methylphenyl)sulfinyl]propionic acid (2) and commercially available perfluorinated esters. Compound (+)-(S)-1b is the pentafluoro analogue of the aggregation pheromone of Trogoderma glabrum.
    DOI:
    10.1002/1099-0690(200206)2002:12<1895::aid-ejoc1895>3.0.co;2-1
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文献信息

  • Stereoselective Synthesis of Both Enantiomers of Trifluoro-γ-valerolactone and Pentafluoro-γ-caprolactone
    作者:Pierfrancesco Bravo、Massimo Frigerio、Alfonso Melloni、Walter Panzeri、Cristina Pesenti、Fiorenza Viani、Matteo Zanda
    DOI:10.1002/1099-0690(200206)2002:12<1895::aid-ejoc1895>3.0.co;2-1
    日期:2002.6
    Both enantiomers of 5-(trifluoromethyl)dihydrofuran-2-one (1a) and 5-(pentafluoroethyl)dihydrofuran-2-one (1b) have been synthesised stereoselectively, in four steps, starting from chiral (R)- or (S)-3-[(4-methylphenyl)sulfinyl]propionic acid (2) and commercially available perfluorinated esters. Compound (+)-(S)-1b is the pentafluoro analogue of the aggregation pheromone of Trogoderma glabrum.
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