6-fluoro-3,4-dihydrophenanthren-(2H)-1-one | 207917-07-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 菲及其衍生物
• 英文名称: 6-fluoro-3,4-dihydrophenanthren-(2H)-1-one
• 英文别名: 6-fluoro-3,4-dihydrophenanthren-1(2H)-one；6-fluoro-3,4-dihydro-2H-phenanthren-1-one
• CAS: 207917-07-5
• 化学式: C₁₄H₁₁FO
• 分子量: 214.239
• InChiKey: CRCTYLHVIFEJFP-UHFFFAOYSA-N

物化性质

• 熔点：
  134-136 °C
• 沸点：
  369.8±11.0 °C(Predicted)
• 密度：
  1.252±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  16
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  6-fluoro-3,4-dihydrophenanthren-(2H)-1-one 在 氢氧化钾 、 正丁基锂 、 二乙胺基三氟化硫 、 一水合肼 、 2,3-二氯-5,6-二氰基-1,4-苯醌 、 copper(ll) bromide 、 lithium tert-butoxide 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 正己烷 、 二氯甲烷 、 甲苯 、 苯 为溶剂， 反应 7.5h， 生成 2-(6-fluorophenanthr-1-yl)-2,3,3,3-tetrafluoropropionic acid
  参考文献：
  名称：

  Regioselectively Nucleus and/or Side-Chain Fluorinated 2-(Phenanthryl)propionic Acids by an Effective Combination of Radical and Organometallic Chemistry

  摘要：

  Regioselectively nucleus and/or side-chain fluorinated 2-(phenanthr-1-yl)- and 2-(phenanthr-2-yl)-propionic acids 1-5 were prepared using phenanthren-1(2H)-ones 6a-c as key intermediates. Thus. ethyl 2-(fluorophenanthryl)propionates 11 were obtained in good yields by Reformatsky reaction of 6a-c with ethyl 2-bromopropionate followed by dehydratation and DDQ-promoted aromatization of the resulting beta-hydroxyesters. Side-chain alkyl 2-hydroxy-2-(phenanthr-1-yl)propionates 14 were obtained by bromine/lithium permutation of dihydrophenanthryl bromides 12a-c with butyllithium followed by quenching of the lithiated intermediates with methyl pyruvate or ethyl 3,3,3-trifluoropyruvate and subsequent DDQ-promoted aromatization. The alkyl 2-hydroxy-2-(phenanthr-1-yl)propionates 25 were prepared by reacting 8-bromo-1,3-difluorophenanthrene 24 with butyllithium for 10 seconds at -110degreesC and subsequent addition of the suitable pyruvate to the lithiated intermediates. Alkyl 2-hydroxy-2-(phenanthr-2-yl)propionates 26 and 29 were suitably obtained by site-selective metalation of 1,3-difluorophenanthrene 28 and the bromophenanthrene 24: respectively, with LDA followed by quenching of the metalated intermediates with the Suitable alkyl pyruvate. Fluorination of the above alpha-hydroxypropionates with DAST, followed by the alkaline hydrolysis, allowed the expected 2-(phenanthryl)propionic acids 1-5 to be obtained in satisfactory overall yields.

  DOI：

  10.1021/jo048294k
• 作为产物：
  描述：

  间溴氟苯 在 ammonium cerium(IV) nitrate 、 calcium carbonate 作用下， 以 甲醇 为溶剂， 反应 1.0h， 生成 6-fluoro-3,4-dihydrophenanthren-(2H)-1-one
  参考文献：
  名称：

  Oxidative Coupling of O-Silyl and O-Alkyl Enethers:  Application of the Novel Annulation Sequence to the Synthesis of Fluorinated Naphthaldehydes and Naphthyl Ketones

  摘要：

  DOI：

  10.1021/jo001006+

文献信息

• A New Synthetic Approach to Substituted 1(2<i>H</i>)-Phenanthrenones Based on the Ceric Ammonium Nitrate-Promoted Oxidative Addition of 3-Aryl-1-[(trimethylsilyl)oxy]- cyclohexenes to Ethyl Vinyl Ether
  作者：Paolo Lupattelli、Renzo Ruzziconi、Patrizia Scafato、Sergio Alunni、Anna Belli Paolobelli

  DOI：10.1021/jo972233n

  日期：1998.6.1
• Oxidative Coupling of <i>O</i>-Silyl and <i>O</i>-Alkyl Enethers:  Application of the Novel Annulation Sequence to the Synthesis of Fluorinated Naphthaldehydes and Naphthyl Ketones
  作者：Jean-Philippe Gourvès、Renzo Ruzziconi、Lluís Vilarroig

  DOI：10.1021/jo001006+

  日期：2001.1.1
• Regioselectively Nucleus and/or Side-Chain Fluorinated 2-(Phenanthryl)propionic Acids by an Effective Combination of Radical and Organometallic Chemistry
  作者：Giacomo Ricci、Renzo Ruzziconi

  DOI：10.1021/jo048294k

  日期：2005.1.1

  Regioselectively nucleus and/or side-chain fluorinated 2-(phenanthr-1-yl)- and 2-(phenanthr-2-yl)-propionic acids 1-5 were prepared using phenanthren-1(2H)-ones 6a-c as key intermediates. Thus. ethyl 2-(fluorophenanthryl)propionates 11 were obtained in good yields by Reformatsky reaction of 6a-c with ethyl 2-bromopropionate followed by dehydratation and DDQ-promoted aromatization of the resulting beta-hydroxyesters. Side-chain alkyl 2-hydroxy-2-(phenanthr-1-yl)propionates 14 were obtained by bromine/lithium permutation of dihydrophenanthryl bromides 12a-c with butyllithium followed by quenching of the lithiated intermediates with methyl pyruvate or ethyl 3,3,3-trifluoropyruvate and subsequent DDQ-promoted aromatization. The alkyl 2-hydroxy-2-(phenanthr-1-yl)propionates 25 were prepared by reacting 8-bromo-1,3-difluorophenanthrene 24 with butyllithium for 10 seconds at -110degreesC and subsequent addition of the suitable pyruvate to the lithiated intermediates. Alkyl 2-hydroxy-2-(phenanthr-2-yl)propionates 26 and 29 were suitably obtained by site-selective metalation of 1,3-difluorophenanthrene 28 and the bromophenanthrene 24: respectively, with LDA followed by quenching of the metalated intermediates with the Suitable alkyl pyruvate. Fluorination of the above alpha-hydroxypropionates with DAST, followed by the alkaline hydrolysis, allowed the expected 2-(phenanthryl)propionic acids 1-5 to be obtained in satisfactory overall yields.