1-(trifluoromethyl)-1-indanol | 121692-27-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 茚满类
• 英文名称: 1-(trifluoromethyl)-1-indanol
• 英文别名: 1-(trifluoromethyl)-2,3-dihydroinden-1-ol
• CAS: 121692-27-1
• 化学式: C₁₀H₉F₃O
• 分子量: 202.176
• InChiKey: RLRMXTVZEDMFHB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  20.2
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  1-(trifluoromethyl)-1-indanol 在 对甲苯磺酸 作用下， 以 苯 为溶剂， 反应 24.0h， 生成 1-(三氟甲基)茚
  参考文献：
  名称：

  Synthesis of perfluoroalkylated indenes

  摘要：

  A series of perfluoroalkylated indenes has been synthesized using four different synthetic pathways. 1-(Pentafluoroethyl)indene and 2-(pentafluoroethyl)indene were prepared by the addition of (pentafluoroethyl)lithium to the appropriate ketones and subsequent dehydration. 2-(Trifluoromethyl)indene was synthesized through the photoinduced addition of trifluoromethyl iodide to indene, followed by dehydroiodination. 1-(Trifluoromethyl)indene was prepared by the addition of (trifluoromethyl)trimethylsilane to 1-indanone followed by deprotection and dehydration and by the sigmatropic cyclization of the appropriate phenylvinyl carbocation. This latter approach was also used to synthesize 1,3-bis(trifluoromethyl)indene and 1,2,3-tris(trifluoromethyl)indene.

  DOI：

  10.1021/jo00017a029
• 作为产物：
  描述：

  1-茚酮 在 四丁基氟化铵 、 (三氟甲基)三甲基硅烷 作用下， 以 四氢呋喃 为溶剂， 反应 20.0h， 以67%的产率得到1-(trifluoromethyl)-1-indanol
  参考文献：
  名称：

  Synthesis of perfluoroalkylated indenes

  摘要：

  A series of perfluoroalkylated indenes has been synthesized using four different synthetic pathways. 1-(Pentafluoroethyl)indene and 2-(pentafluoroethyl)indene were prepared by the addition of (pentafluoroethyl)lithium to the appropriate ketones and subsequent dehydration. 2-(Trifluoromethyl)indene was synthesized through the photoinduced addition of trifluoromethyl iodide to indene, followed by dehydroiodination. 1-(Trifluoromethyl)indene was prepared by the addition of (trifluoromethyl)trimethylsilane to 1-indanone followed by deprotection and dehydration and by the sigmatropic cyclization of the appropriate phenylvinyl carbocation. This latter approach was also used to synthesize 1,3-bis(trifluoromethyl)indene and 1,2,3-tris(trifluoromethyl)indene.

  DOI：

  10.1021/jo00017a029

文献信息

• [EN] ARYL ETHERS AND USES THEREOF<br/>[FR] ARYLÉTHERS ET UTILISATIONS DE CEUX-CI
  申请人：PELOTON THERAPEUTICS INC

  公开号：WO2015035223A1

  公开（公告）日：2015-03-12

  The present disclosure relates to HIF-2α inhibitors and methods of making and using them for treating cancer. Certain compounds were potent in HIF-2α scintillation proximity assay, luciferase assay, and VEGF ELISA assay, and led to tumor size reduction and regression in 786-O xenograft bearing mice in vivo.

  本公开涉及HIF-2α抑制剂及其制备和用于治疗癌症的方法。某些化合物在HIF-2α闪烁近距离法、荧光素酶法和VEGF ELISA法中表现出强效，导致786-O异种移植瘤小鼠体内肿瘤大小减小和回归。
• Aubert, Corinne; Begue, Jean-Pierre; Bonnet-Delpon, Daniele, Journal of the Chemical Society. Perkin transactions I, 1989, p. 395 - 399
  作者：Aubert, Corinne、Begue, Jean-Pierre、Bonnet-Delpon, Daniele、Mesureur, Dany

  DOI：——

  日期：——
• AUBERT, CORINNE;BEGUE, JEAN-PIERRE;BONNET-DELPON, DANIELE;MESUREUR, DANY, J. CHEM. SOC. PERKIN TRANS. PT 1,(1989) N, C. 395-399
  作者：AUBERT, CORINNE、BEGUE, JEAN-PIERRE、BONNET-DELPON, DANIELE、MESUREUR, DANY

  DOI：——

  日期：——
• ARYL ETHERS AND USES THEREOF
  申请人：Peloton Therapeutics, Inc.

  公开号：EP3043784A1

  公开（公告）日：2016-07-20
• Synthesis of perfluoroalkylated indenes
  作者：Paul G. Gassman、Julia A. Ray、Paul G. Wenthold、John W. Mickelson

  DOI：10.1021/jo00017a029

  日期：1991.8

  A series of perfluoroalkylated indenes has been synthesized using four different synthetic pathways. 1-(Pentafluoroethyl)indene and 2-(pentafluoroethyl)indene were prepared by the addition of (pentafluoroethyl)lithium to the appropriate ketones and subsequent dehydration. 2-(Trifluoromethyl)indene was synthesized through the photoinduced addition of trifluoromethyl iodide to indene, followed by dehydroiodination. 1-(Trifluoromethyl)indene was prepared by the addition of (trifluoromethyl)trimethylsilane to 1-indanone followed by deprotection and dehydration and by the sigmatropic cyclization of the appropriate phenylvinyl carbocation. This latter approach was also used to synthesize 1,3-bis(trifluoromethyl)indene and 1,2,3-tris(trifluoromethyl)indene.