2,2-bis({[tert-butyl(dimethyl)silyl]oxy}methyl)-6-phenyl-4H-1,3-dioxin-4-one

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,2-bis({[tert-butyl(dimethyl)silyl]oxy}methyl)-6-phenyl-4H-1,3-dioxin-4-one
• 英文别名: 2,2-Bis[[tert-butyl(dimethyl)silyl]oxymethyl]-6-phenyl-1,3-dioxin-4-one
• 化学式: C₂₄H₄₀O₅Si₂
• 分子量: 464.75
• InChiKey: BVUHGCLTNFCHHK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.34
• 重原子数：
  31
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  54
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2,2-bis({[tert-butyl(dimethyl)silyl]oxy}methyl)-6-phenyl-4H-1,3-dioxin-4-one 在 三氟乙酸 作用下， 以 甲醇 为溶剂， 反应 40.0h， 以93%的产率得到2,2-bis(hydroxymethyl)-6-phenyl-4H-1,3-dioxin-4-one
  参考文献：
  名称：

  Synthesis of optically active 1,3-dioxin-4-one derivatives having a hydroxymethyl group at the 2-position and their use for regio-, diastereo-, and enantioselective synthesis of substituted cyclobutanols

  摘要：

  A new method for preparing optically active 1,3-dioxin-4-one derivatives is presented. A series of prochiral 2,2-bis(hydroxymethyl)-1,3-dioxin-4-ones was synthesized by [4+2]cycloaddition of acylketene to protected 1,3-dihydroxy-2-propanone derivatives followed by deprotection of the hydroxyl groups. Desymmetrization of the prochiral dioxinones by lipase-catalyzed monoacetylation afforded optically active 2-(hydroxymethyl)dioxin ones. Intramolecular photo[2+2]cycloaddition of W-alkenyl esters of these alcohols provided an efficient method for regio-, diastereo-, and enantio selective synthesis of cyclobutanols. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(02)00760-7
• 作为产物：
  描述：

  1,3-bis-O-(tert-butyldimethylsilyl)-1,3-dihydroxy-2-propanone 、 5-benzoyl-2,2-dimethyl-1,3-dioxane-4,6-dione 以 甲苯 为溶剂， 反应 1.0h， 以65%的产率得到2,2-bis({[tert-butyl(dimethyl)silyl]oxy}methyl)-6-phenyl-4H-1,3-dioxin-4-one
  参考文献：
  名称：

  Synthesis of optically active 1,3-dioxin-4-one derivatives having a hydroxymethyl group at the 2-position and their use for regio-, diastereo-, and enantioselective synthesis of substituted cyclobutanols

  摘要：

  A new method for preparing optically active 1,3-dioxin-4-one derivatives is presented. A series of prochiral 2,2-bis(hydroxymethyl)-1,3-dioxin-4-ones was synthesized by [4+2]cycloaddition of acylketene to protected 1,3-dihydroxy-2-propanone derivatives followed by deprotection of the hydroxyl groups. Desymmetrization of the prochiral dioxinones by lipase-catalyzed monoacetylation afforded optically active 2-(hydroxymethyl)dioxin ones. Intramolecular photo[2+2]cycloaddition of W-alkenyl esters of these alcohols provided an efficient method for regio-, diastereo-, and enantio selective synthesis of cyclobutanols. (C) 2003 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0957-4166(02)00760-7

文献信息

• Synthesis of optically active 1,3-dioxin-4-one derivatives having a hydroxymethyl group at the 2-position and their use for regio-, diastereo-, and enantioselective synthesis of substituted cyclobutanols
  作者：Masayuki Murakami、Hiroshi Kamaya、Chikara Kaneko、Masayuki Sato

  DOI：10.1016/s0957-4166(02)00760-7

  日期：2003.1

  A new method for preparing optically active 1,3-dioxin-4-one derivatives is presented. A series of prochiral 2,2-bis(hydroxymethyl)-1,3-dioxin-4-ones was synthesized by [4+2]cycloaddition of acylketene to protected 1,3-dihydroxy-2-propanone derivatives followed by deprotection of the hydroxyl groups. Desymmetrization of the prochiral dioxinones by lipase-catalyzed monoacetylation afforded optically active 2-(hydroxymethyl)dioxin ones. Intramolecular photo[2+2]cycloaddition of W-alkenyl esters of these alcohols provided an efficient method for regio-, diastereo-, and enantio selective synthesis of cyclobutanols. (C) 2003 Elsevier Science Ltd. All rights reserved.