(+/-)-1-(5-phenyl-2H-tetrazol-2-yl)propan-2-ol | 93742-44-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: (+/-)-1-(5-phenyl-2H-tetrazol-2-yl)propan-2-ol
• 英文别名: 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-ol；2-(2-hydroxypropyl)-5-phenyltetrazole；1-(5-phenyltetrazol-2-yl)propan-2-ol；I+/--Methyl-5-phenyl-2H-tetrazole-2-ethanol
• CAS: 93742-44-0
• 化学式: C₁₀H₁₂N₄O
• 分子量: 204.231
• InChiKey: IXROSBYQUSKQKE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  63.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  乙酸酐 、 (+/-)-1-(5-phenyl-2H-tetrazol-2-yl)propan-2-ol 在 吡啶 作用下， 反应 24.0h， 生成 1-(5-phenyltetrazol-2-yl)propan-2-yl acetate
  参考文献：
  名称：

  Lipase-catalyzed enantioseparation of alcohols containing a tetrazole ring

  摘要：

  A simple chemoenzymatic method for the preparation of optically active (5-aryltetrazolyl-2)-4-butan-2-ol, (5-aryltetrazolyl-2)-propan-2-ol, and their acetates has been developed. The starting compounds (5-aryltetrazolyl-2)-4-butan-2-one and (5-aryltetrazolyl-2)-propan-2-one were obtained by a Michael-type addition of 5-aryl substituted tetrazoles to methyl vinyl ketone, and alkylation of 5-aryl substituted tetrazoles with chloroacetone, respectively. Their reduction with sodium borohydride afforded racemic mixtures of (5-aryltetrazolyl-2)-4-butan-2-oles and (5-aryltetrazolyl-2)-propan-2-oles. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2012.01.015
• 作为产物：
  描述：

  5-苯基四氮唑 在 三乙胺 、 蔗糖 作用下， 以 水 、 乙腈 为溶剂， 反应 102.5h， 生成 (+/-)-1-(5-phenyl-2H-tetrazol-2-yl)propan-2-ol
  参考文献：
  名称：

  四唑基烷醇和四唑基（羟基）烷基膦酸酯的合成中的5-苯基-2 H-四唑-2-基甲基酮

  摘要：

  用四氢硼酸钠还原1-（5-苯基-2 H-四唑-2-基）丙-2-酮和1-苯基-2-（5-苯基-2 H-四唑-2-基）乙酮得到1-（5-苯基-2 H-四唑-2-基）丙-1-醇和1-苯基-2-（5-苯基-2 H-四唑-2-基）乙醇。面包酵母仅还原了1-（5-苯基-2 H-四唑-2-基）丙-2-酮，收率相当可观。1-（5-苯基-2 H-四唑-2-基）丙-2-酮和1-苯基-2-（5-苯基-2 H-四唑-2-基）乙酮在存在下与膦酸二乙酯反应氟化钾生成相应的[羟基（5-苯基-2 H-四唑-2-基）烷基]二乙基膦酸酯。

  DOI：

  10.1134/s1070428014060219

文献信息

• Casey, Michael; Moody, Christopher J.; Rees, Charles W., Journal of the Chemical Society. Perkin transactions I, 1984, # 8, p. 1933 - 1941
  作者：Casey, Michael、Moody, Christopher J.、Rees, Charles W.

  DOI：——

  日期：——
• CASEY, M.;MOODY, CH. J.;REES, CH. W., J. CHEM. SOC. PERKIN TRANS., 1984, N 8, 1933-1941
  作者：CASEY, M.、MOODY, CH. J.、REES, CH. W.

  DOI：——

  日期：——
• 5-phenyl-2H-tetrazol-2-ylmethyl ketones in the synthesis of tetrazolylalkanols and tetrazolyl(hydroxy)alkylphosphonates
  作者：A. S. Krylov、A. V. Dogadina、R. E. Trifonov

  DOI：10.1134/s1070428014060219

  日期：2014.6

  ne and 1-phenyl-2-(5-phenyl-2H-tetrazol-2-yl)ethanone with sodium tetrahydridoborate gave 1-(5-phenyl-2H-tetrazol-2-yl)propan-1-ol and 1-phenyl-2-(5-phenyl-2H-tetrazol-2-yl)ethanol, respectively. Only 1-(5-phenyl-2H-tetrazol-2-yl)propan-2-one was reduced with baker’s yeast with an appreciable yield. 1-(5-Phenyl-2H-tetrazol-2-yl)propan-2-one and 1-phenyl-2-(5-phenyl-2H-tetrazol-2-yl)ethanone reacted

  用四氢硼酸钠还原1-（5-苯基-2 H-四唑-2-基）丙-2-酮和1-苯基-2-（5-苯基-2 H-四唑-2-基）乙酮得到1-（5-苯基-2 H-四唑-2-基）丙-1-醇和1-苯基-2-（5-苯基-2 H-四唑-2-基）乙醇。面包酵母仅还原了1-（5-苯基-2 H-四唑-2-基）丙-2-酮，收率相当可观。1-（5-苯基-2 H-四唑-2-基）丙-2-酮和1-苯基-2-（5-苯基-2 H-四唑-2-基）乙酮在存在下与膦酸二乙酯反应氟化钾生成相应的[羟基（5-苯基-2 H-四唑-2-基）烷基]二乙基膦酸酯。
• Lipase-catalyzed enantioseparation of alcohols containing a tetrazole ring
  作者：Edyta Łukowska-Chojnacka、Urszula Bernaś、Jan Plenkiewicz

  DOI：10.1016/j.tetasy.2012.01.015

  日期：2012.1

  A simple chemoenzymatic method for the preparation of optically active (5-aryltetrazolyl-2)-4-butan-2-ol, (5-aryltetrazolyl-2)-propan-2-ol, and their acetates has been developed. The starting compounds (5-aryltetrazolyl-2)-4-butan-2-one and (5-aryltetrazolyl-2)-propan-2-one were obtained by a Michael-type addition of 5-aryl substituted tetrazoles to methyl vinyl ketone, and alkylation of 5-aryl substituted tetrazoles with chloroacetone, respectively. Their reduction with sodium borohydride afforded racemic mixtures of (5-aryltetrazolyl-2)-4-butan-2-oles and (5-aryltetrazolyl-2)-propan-2-oles. (C) 2012 Elsevier Ltd. All rights reserved.