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2-(2-Thienyl)-6-tert-butyl-4H-thiopyran-4-one | 156147-06-7

中文名称
——
中文别名
——
英文名称
2-(2-Thienyl)-6-tert-butyl-4H-thiopyran-4-one
英文别名
2-(thien-2-yl)-6-t-butyl-4H-thiopyran-4-one;2-(2-thienyl)-6-t-butyl-4H-thiopyran-4-one;2-Tert-butyl-6-thiophen-2-ylthiopyran-4-one
2-(2-Thienyl)-6-tert-butyl-4H-thiopyran-4-one化学式
CAS
156147-06-7
化学式
C13H14OS2
mdl
——
分子量
250.386
InChiKey
SWZZWEVJHBELTJ-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):
    3.7
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    70.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-(2-Thienyl)-6-tert-butyl-4H-thiopyran-4-one过氧乙酸 作用下, 以 溶剂黄146乙酸乙酯 为溶剂, 反应 3.0h, 以39%的产率得到2-(2-Thienyl)-6-tert-butyl-4H-thiopyran-4-one 1,1-dioxide
    参考文献:
    名称:
    Syntheses of 4H-Thiopyran-4-one 1,1-Dioxides as Precursors to Sulfone-Containing Analogs of Tetracyanoquinodimethane
    摘要:
    Synthetic routes to the unsubstituted 4H-thiopyran-4-one 1,1-dioxide (5a), 2,6-dialkyl-substituted, 2-aryl- or 2-heteroaryl-6-alkyl-substituted, 2,6-diaryl- or diheteroaryl-substituted, and 2-heteroaryl-6-aryl-substituted 4H-thiopyran-4-one 1,1-dioxides 5b-s are described. Sodium hydrosulfide hydrate in buffered aqueous alcohol can be used as a substitute for hydrogen sulfide gas for the introduction of sulfur to methyl acrylate, to 1,5-disubstituted-1,4-pentadien-3-ones 13, or to 1,5-disubstituted-1,4-pentadiyn-3-ones 17. The double dehydrogenation af 2,3,5,6-tetrahydrothiopyran-4-one 1,1-dioxides 13 with iodine-DMSO-sulfuric acid gives thiopyran-4-one 1,1-dioxides 5 in good yield and small amounts of 1,4-pentadien-3-ones 13. 2,3,5,6-Tetrahydrothiopyran-4-one 1,1-dioxide (9) and 5,6-dihydrothiopyran-4-one 1,1-dioxide (12), which lack aryl or heteroaryl substituents, give poor yields of 4H-thiopyran-4-one 1,1-dioxide (5a) with iodine-DMSO-sulfuric acid.
    DOI:
    10.1021/jo00111a027
  • 作为产物:
    描述:
    thiophen-2-yl-propynalsodium hydrogensulfide正丁基锂 、 sodium dichromate 、 硫酸碳酸氢钠 作用下, 以 四氢呋喃乙醇正己烷丙酮 为溶剂, 反应 16.0h, 生成 2-(2-Thienyl)-6-tert-butyl-4H-thiopyran-4-one
    参考文献:
    名称:
    Syntheses of 4H-Thiopyran-4-one 1,1-Dioxides as Precursors to Sulfone-Containing Analogs of Tetracyanoquinodimethane
    摘要:
    Synthetic routes to the unsubstituted 4H-thiopyran-4-one 1,1-dioxide (5a), 2,6-dialkyl-substituted, 2-aryl- or 2-heteroaryl-6-alkyl-substituted, 2,6-diaryl- or diheteroaryl-substituted, and 2-heteroaryl-6-aryl-substituted 4H-thiopyran-4-one 1,1-dioxides 5b-s are described. Sodium hydrosulfide hydrate in buffered aqueous alcohol can be used as a substitute for hydrogen sulfide gas for the introduction of sulfur to methyl acrylate, to 1,5-disubstituted-1,4-pentadien-3-ones 13, or to 1,5-disubstituted-1,4-pentadiyn-3-ones 17. The double dehydrogenation af 2,3,5,6-tetrahydrothiopyran-4-one 1,1-dioxides 13 with iodine-DMSO-sulfuric acid gives thiopyran-4-one 1,1-dioxides 5 in good yield and small amounts of 1,4-pentadien-3-ones 13. 2,3,5,6-Tetrahydrothiopyran-4-one 1,1-dioxide (9) and 5,6-dihydrothiopyran-4-one 1,1-dioxide (12), which lack aryl or heteroaryl substituents, give poor yields of 4H-thiopyran-4-one 1,1-dioxide (5a) with iodine-DMSO-sulfuric acid.
    DOI:
    10.1021/jo00111a027
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文献信息

  • US5300385A
    申请人:——
    公开号:US5300385A
    公开(公告)日:1994-04-05
  • US5352802A
    申请人:——
    公开号:US5352802A
    公开(公告)日:1994-10-04
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