4-[4-(1,1-dimethylethyl)phenyl]-2-oxo-thiazole | 127740-03-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-[4-(1,1-dimethylethyl)phenyl]-2-oxo-thiazole
• 英文别名: 4-(4-t-Butyl-phenyl)-3h-thiazol-2-one；4-(4-tert-butylphenyl)-3H-1,3-thiazol-2-one
• CAS: 127740-03-8
• 化学式: C₁₃H₁₅NOS
• mdl: MFCD11220422
• 分子量: 233.334
• InChiKey: RCFZDEALNDPTKG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  16
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.307
• 拓扑面积：
  54.4
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  4-甲酰-15-冠-5 、 4-[4-(1,1-dimethylethyl)phenyl]-2-oxo-thiazole 在 硫酸 作用下， 以 溶剂黄146 为溶剂， 以72%的产率得到4-(4-tert-butylphenyl)-5-[[4-(4-tert-butylphenyl)-2-oxo-3H-1,3-thiazol-5-yl]-(2,5,8,11,14-pentaoxabicyclo[13.4.0]nonadeca-1(15),16,18-trien-17-yl)methyl]-3H-1,3-thiazol-2-one
  参考文献：
  名称：

  Teller, Joachim; Holdt, Hans-Juergen; Dehne, Heinz, Zeitschrift fur Chemie, 1989, vol. 29, # 12, p. 446 - 447

  摘要：

  DOI：
• 作为产物：
  描述：

  1-(4-(tert-butyl)phenyl)-2-thiocyanatoethan-1-one 在 盐酸 作用下， 以 水 为溶剂， 反应 3.0h， 以163 mg的产率得到4-[4-(1,1-dimethylethyl)phenyl]-2-oxo-thiazole
  参考文献：
  名称：

  末端炔烃1，，3-芳基二烯的光敏氧硫氰化反应及其一锅法转化为2-羟基4-取代的芳基噻唑

  摘要：

  从活化的末端芳基炔烃和芳基1,3-共轭二烯实现了区域选择性可见光诱导的芳基α-硫氰基酮/硫氰基醇的合成。在有机光催化剂和NH 4 SCN的存在下，这种温和且非金属的氧化仅由良性环境空气驱动。还以5 mmol的规模证明了该方案，可以高收率合成潜在的治疗性2-羟基4-取代的芳基噻唑，表明其可大规模应用。

  DOI：

  10.1039/c9ob00054b

文献信息

• A correlative IR, MS, 1H, 13C and 15N NMR and theoretical study of 4-arylthiazol-2(3H)-onesElectronic supplementary information (ESI) available: NMR data, including graphs; Cartesian coordinates for 3a and 4. See http://www.rsc.org/suppdata/p2/b1/b106322g/
  作者：Kalevi Pihlaja、Vladimir Ovcharenko、Erkki Kolehmainen、Katri Laihia、Walter M. F. Fabian、Heinz Dehne、Alexander Perjéssy、Marion Kleist、Joachim Teller、Zora Šusteková

  DOI：10.1039/b106322g

  日期：2002.1.23

  Sixteen 4-arylthiazol-2(3H)-ones (3) were synthesised by cyclisation of α-thiocyanatoacetophenones (1) in acid solution. They appear to prefer greatly the oxo tautomeric forms. In CCl4 solution an equilibrium between the free CO bond and a “dimeric” hydrogen-bonded form exists in which the latter predominates. Several IR and NMR (1H, 13C and 15N) spectral properties are shown to correlate with Hammett σ-values and/or atomic Mulliken charges and bond orders, the latter being estimated by PM3 or AM1 semiempirical methods. The electron-impact mass spectra were also recorded and the fragmentation mechanisms interpreted in terms of the energetics of the ionic species. In addition, the geometric and electronic properties of 4-phenylthiazol-2(3H)-one (3a) and the related benzothiazol-2(3H)-one (4) based on ab initio HF/6-31 G* calculations are compared with each other.

  通过在酸性溶液中环化α-硫氰基苯乙酮（1），合成了16种4-芳基噻唑-2(3H)-酮（3）。它们似乎更倾向于氧代互变异构形式。在CCl4溶液中，自由羰基键与“二聚”氢键形式之间存在平衡，其中后者占优势。有几种红外和核磁共振（1H、13C和15N）光谱特性与Hammett σ值和/或原子Mulliken电荷及键级相关联，后者通过PM3或AM1半经验方法估算。还记录了电子冲击质谱，并根据离子物种的能量学解释了裂解机制。此外，基于从头算HF/6-31G*计算，比较了4-苯基噻唑-2(3H)-酮（3a）及相关苯并噻唑-2(3H)-酮（4）的几何和电子性质。
• [EN] TETRAZOLINONE COMPOUNDS AND ITS USE<br/>[FR] COMPOSÉS DE TÉTRAZOLINONE ET LEUR UTILISATION
  申请人：SUMITOMO CHEMICAL CO

  公开号：WO2013162077A1

  公开（公告）日：2013-10-31

  The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein, R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, a C3-C12 cycloalkyl group or an adamantyl group, etc., which each optionally be substituted; R2 represents a hydrogen atom, an C1-C12 alkyl group, or a halogen atom, etc.; R4 and R5 represent independently of each other a hydrogen atom or an C1-C3 alkyl group, etc.; R6, R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, an C1-C12 alkyl group, a C1-C12 haloalkyl group, an C2-C12 alkenyl group, a C3-C12 cycloalkyl group, an C1-C12 alkoxy group or a C1-C12 haloalkoxy group, etc.; X and Y represent independently of each other a sulfur atom or an oxygen atom; Q represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.

  本发明提供了一种具有优异杀虫效果的化合物。式（1）中的四氮杂酮化合物：[其中，R1代表一个C6-C16芳基，一个C1-C12烷基，一个C3-C12环烷基或一个金刚烷基等，每个都可以选择性地被取代；R2代表一个氢原子，一个C1-C12烷基或一个卤素原子等；R4和R5分别独立地代表一个氢原子或一个C1-C3烷基等；R6、R7、R8和R9分别独立地代表一个氢原子，一个卤素原子，一个C1-C12烷基，一个C1-C12卤代烷基，一个C2-C12烯基，一个C3-C12环烷基，一个C1-C12烷氧基或一个C1-C12卤代烷氧基等；X和Y分别独立地代表一个硫原子或一个氧原子；Q代表一个氧原子或一个硫原子；R10代表一个C1-C6烷基等]对害虫有极佳的控制效果。
• TETRAZOLINONE COMPOUNDS AND ITS USE
  申请人：SUMITOMO CHEMICAL COMPANY, LIMITED

  公开号：US20150031733A1

  公开（公告）日：2015-01-29

  The present invention provides a compound having an excellent efficacy for controlling pests. A tetrazolinone compound of a formula (1): [wherein, R1 represents an C6-C16 aryl group, an C1-C12 alkyl group, a C3-C12 cycloalkyl group or an adamantyl group, etc., which each optionally be substituted; R2 represents a hydrogen atom, an C1-C12 alkyl group, or a halogen atom, etc.; R4 and R5 represent independently of each other a hydrogen atom or an C1-C3 alkyl group, etc.; R6, R7, R8 and R9 represent independently of each other a hydrogen atom, a halogen atom, an C1-C12 alkyl group, a C1-C12 haloalkyl group, an C2-C12 alkenyl group, a C3-C12 cycloalkyl group, an C1-C12 alkoxy group or a C1-C12 haloalkoxy group, etc.; X and Y represent independently of each other a sulfur atom or an oxygen atom; Q represents an oxygen atom or a sulfur atom; and R10 represents an C1-C6 alkyl group, etc.] shows an excellent controlling efficacy on pests.

  本发明提供了一种具有优异的杀虫功效的化合物。公式（1）的四唑酮化合物：[其中，R1代表C6-C16芳基，C1-C12烷基，C3-C12环烷基或金刚烷基等，每个都可以选择性地被取代；R2代表氢原子，C1-C12烷基或卤素原子等；R4和R5分别独立地代表氢原子或C1-C3烷基等；R6、R7、R8和R9分别独立地代表氢原子、卤素原子、C1-C12烷基、C1-C12卤代烷基、C2-C12烯基、C3-C12环烷基、C1-C12烷氧基或C1-C12卤代烷氧基等；X和Y分别独立地代表硫原子或氧原子；Q代表氧原子或硫原子；R10代表C1-C6烷基等]在控制害虫方面表现出优异的效果。
• TELLER, JOACHIM;DEHNE, HEINZ
  作者：TELLER, JOACHIM、DEHNE, HEINZ

  DOI：——

  日期：——
• US9380782B2
  申请人：——

  公开号：US9380782B2

  公开（公告）日：2016-07-05