摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

4-(4-fluorophenylsulfanyl)-3-hydroxy-2-pyrone | 881171-81-9

中文名称
——
中文别名
——
英文名称
4-(4-fluorophenylsulfanyl)-3-hydroxy-2-pyrone
英文别名
4-(4-fluorophenyl)sulfanyl-3-hydroxypyran-2-one
4-(4-fluorophenylsulfanyl)-3-hydroxy-2-pyrone化学式
CAS
881171-81-9
化学式
C11H7FO3S
mdl
——
分子量
238.239
InChiKey
LYWQPUBYDLGNMO-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):
    2.5
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    71.8
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    4-(4-fluorophenylsulfanyl)-3-hydroxy-2-pyrone丁炔二酸二甲酯三乙胺 作用下, 以 氯仿 为溶剂, 反应 2.0h, 以87%的产率得到dimethyl 4-(4-fluorophenylthio)-3-hydroxyphthalate
    参考文献:
    名称:
    Synthesis of 4‐Arylthio‐3‐hydroxyphthalate by the Diels–Alder Reactionof 4‐Arylthio‐3‐hydroxy‐2‐pyrone
    摘要:
    Treatment of 4-arylthio-3-hydroxy-2-pyrones with acetylenedicarboxylates gave 4-arylthio-3-hydroxyphthalates by the base-catalyzed Diels-Alder reaction via a decarboxylation in good yields.
    DOI:
    10.1080/00397910601055016
  • 作为产物:
    描述:
    methyl 2-chloro-3-(2,2-dimethyl-1,3-dioxolan-4-yl)oxirane-2-carboxylate4-氟苯硫酚钠盐甲醇 为溶剂, 反应 1.0h, 以84%的产率得到4-(4-fluorophenylsulfanyl)-3-hydroxy-2-pyrone
    参考文献:
    名称:
    Novel Synthesis of 4-Arylsulfenyl-3-hydroxy-2-pyrone: One Pot Substitution-Rearrangement-Cyclization Reaction of Acetonide Protected 4,5-Dihydroxy-2-chloroglycidic Ester by Sodium Arylthiolate
    摘要:
    DOI:
    10.3987/com-05-s(k)60
点击查看最新优质反应信息

文献信息

  • One‐Pot Synthesis of 2‐Arylthio‐2‐cyclohexenone Derivatives by the Diels–Alder Reaction of 4‐Arylthio‐3‐hydroxy‐2‐pyrones
    作者:Takuzo Komiyama、Yutaka Takaguchi、Sadao Tsuboi
    DOI:10.1080/00397910701392434
    日期:2007.7.1
    The base-catalyzed Diels-Alder reactions of 4-arylthio-3- hydroxy-2-pyrones are reported. Treatment of 4-arylthio-3- hydroxy-2-pyrones and dienophiles with triethylamine gave 2-arylthio-2-cyclohexenone derivatives by the Diels-Alder reaction involving a decarboxylation in excellent to reasonable yields.
  • Novel Synthesis of 4-Arylsulfenyl-3-hydroxy-2-pyrone: One Pot Substitution-Rearrangement-Cyclization Reaction of Acetonide Protected 4,5-Dihydroxy-2-chloroglycidic Ester by Sodium Arylthiolate
    作者:Sadao Tsuboi、Takuzo Komiyama、Yutaka Takaguchi
    DOI:10.3987/com-05-s(k)60
    日期:——
  • Synthesis of 4‐Arylthio‐3‐hydroxyphthalate by the Diels–Alder Reactionof 4‐Arylthio‐3‐hydroxy‐2‐pyrone
    作者:Takuzo Komiyama、Yutaka Takaguchi、Sadao Tsuboi
    DOI:10.1080/00397910601055016
    日期:2007.3
    Treatment of 4-arylthio-3-hydroxy-2-pyrones with acetylenedicarboxylates gave 4-arylthio-3-hydroxyphthalates by the base-catalyzed Diels-Alder reaction via a decarboxylation in good yields.
查看更多