di-tert-butyl-methyl-(3,3,3-trifluoro-2-oxa-2-trifluoromethyl-propyl)phosphoniumbetaine | 946535-73-5

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 有机溴化物
• 英文名称: di-tert-butyl-methyl-(3,3,3-trifluoro-2-oxa-2-trifluoromethyl-propyl)phosphoniumbetaine
• CAS: 946535-73-5
• 化学式: C₁₃H₂₃F₆OP
• 分子量: 340.289
• InChiKey: ZVBHPHAYXOJERZ-UHFFFAOYSA-N

反应信息

• 作为反应物：
  描述：

  di-tert-butyl-methyl-(3,3,3-trifluoro-2-oxa-2-trifluoromethyl-propyl)phosphoniumbetaine 190.0 ℃ 、1.33 Pa 条件下， 反应 48.0h， 以71%的产率得到3-(di-tert-butyl-methyl-λ⁵-phosphanylidene)-1,1,1-trifluoro-propan-2-one
  参考文献：
  名称：

  A Stabilized β-Oxaphosphoniumbetaine:  An Elusive Zwitterion

  摘要：

  A beta-oxaphosphoniumbetaine stabilized by two tert-butyl groups at the phosphonium part of the betaine and two trifluoromethyl groups at the carbon adjoined to the oxa part of the betaine was isolated and structurally characterized. Additional stabilization results from the solvation of the betaine by a parent phosphonium salt, as in 4, or by protonation with methanol, as in 10. According to X-ray analysis, the betaine exhibits a sterically strained "gauche" conformeric form, with torsion angles in the P-C-C-O moiety of 32.2 degrees for 4 and 28.1 degrees for 10. The P center dot center dot center dot O separations of 3.121 angstrom for 4 and 3.086 angstrom for 10 are just under the sum of the O and P van der Waals radii (3.32 angstrom). The fast H/D exchange of alpha hydrogen atoms to the phosphonium center was observed in the solution of 10 in deuterium oxide and MeOH-d(4). The beta-oxaphosphoniumbetaine has long been suspected as an intermediate in the Wittig reaction, but this is the first time a stabilized derivative has been isolated.

  DOI：

  10.1021/ja071644a
• 作为产物：
  描述：

  2-[(di-tert-butyl-phosphanyl)methyl]-1,1,1,3,3,3-hexafluoropropan-2-ol 在 sodium hydroxide 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 504072.0h， 生成 di-tert-butyl-methyl-(3,3,3-trifluoro-2-oxa-2-trifluoromethyl-propyl)phosphoniumbetaine
  参考文献：
  名称：

  A Stabilized β-Oxaphosphoniumbetaine:  An Elusive Zwitterion

  摘要：

  A beta-oxaphosphoniumbetaine stabilized by two tert-butyl groups at the phosphonium part of the betaine and two trifluoromethyl groups at the carbon adjoined to the oxa part of the betaine was isolated and structurally characterized. Additional stabilization results from the solvation of the betaine by a parent phosphonium salt, as in 4, or by protonation with methanol, as in 10. According to X-ray analysis, the betaine exhibits a sterically strained "gauche" conformeric form, with torsion angles in the P-C-C-O moiety of 32.2 degrees for 4 and 28.1 degrees for 10. The P center dot center dot center dot O separations of 3.121 angstrom for 4 and 3.086 angstrom for 10 are just under the sum of the O and P van der Waals radii (3.32 angstrom). The fast H/D exchange of alpha hydrogen atoms to the phosphonium center was observed in the solution of 10 in deuterium oxide and MeOH-d(4). The beta-oxaphosphoniumbetaine has long been suspected as an intermediate in the Wittig reaction, but this is the first time a stabilized derivative has been isolated.

  DOI：

  10.1021/ja071644a