4-methoxy-2-(4-methoxy-2-t-butylphenoxy)-6-t-butylphenol | 20236-47-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-methoxy-2-(4-methoxy-2-t-butylphenoxy)-6-t-butylphenol
• 英文别名: 2',3-di-tert-butyl-2-hydorxy-4',5-dimethoxy biphenyl ether；2-(1,1-Dimethylethyl)-6-[2-(1,1-dimethylethyl)-4-methoxyphenoxy]-4-methoxyphenol；2-tert-butyl-6-(2-tert-butyl-4-methoxyphenoxy)-4-methoxyphenol
• CAS: 20236-47-9
• 化学式: C₂₂H₃₀O₄
• 分子量: 358.478
• InChiKey: PDOBLUUAAQFNBA-UHFFFAOYSA-N

物化性质

• 熔点：
  73-76 °C(Solv: methanol (67-56-1))
• 沸点：
  429.7±45.0 °C(Predicted)
• 密度：
  1.054±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  26
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  47.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2,2'-Dihydroxy-5,5'-dimethoxy-4,4'-di-tert.butylbiphenyl 、 4-methoxy-2-(4-methoxy-2-t-butylphenoxy)-6-t-butylphenol 在 sodium hydroxide 、 potassium hexacyanoferrate(III) 作用下， 以 四氯化碳 为溶剂， 以76%的产率得到2,4',10-Trimethoxy-3,6',9-tri-t-butyl-dibenzodioxepin-6-spiro-2'-cyclohexadien-3',5'-on
  参考文献：
  名称：

  Hewgill, Frank R.; Legge, Frank, Journal of the Chemical Society. Perkin transactions I, 1982, # 12, p. 2863 - 2866

  摘要：

  DOI：
• 作为产物：
  描述：

  叔丁基对羟基茴香醚 在 sodium hydroxide 、 potassium hexacyanoferrate(III) 作用下， 以 四氯化碳 为溶剂， 反应 2.0h， 以0.65 g的产率得到4-methoxy-2-(4-methoxy-2-t-butylphenoxy)-6-t-butylphenol
  参考文献：
  名称：

  Hewgill, Frank R.; Legge, Frank, Journal of the Chemical Society. Perkin transactions I, 1982, # 12, p. 2863 - 2866

  摘要：

  DOI：

文献信息

• PROCESS FOR PREPARING 2,2'-DIHYDROXY-3,3'-DI-TERT-BUTYL-5,5'-DIMETHOXY-1,1'-BIPHENOL
  申请人：EVONIK DEGUSSA GMBH

  公开号：US20160340280A1

  公开（公告）日：2016-11-24

  Process for preparing 2,2′-dihydroxy-3,3′-di-tert-butyl-5,5′-dimethoxy-1,1′-biphenol.

  制备2,2'-二羟基-3,3'-二叔丁基-5,5'-二甲氧基-1,1'-联苯酚的过程。
• VERFAHREN ZUR HERSTELLUNG VON 2,2'-DIHYDROXY-3,3'-DI-TERT-BUTYL-5,5'-DIMETHOXY-1,1'-BIPHENOL
  申请人：Evonik Degussa GmbH

  公开号：EP3095775A1

  公开（公告）日：2016-11-23

  Verfahren zur Herstellung von 2,2'-Dihydroxy-3,3'-di-tert.-butyl-5,5'-dimethoxy-1,1'-biphenol.

  2,2'-二羟基-3,3'-二叔丁基-5,5'-二甲氧基-1,1'-联苯酚的制备工艺。
• Mechanism of the Gibbs Reaction. 3. Indophenol Formation via Radical Electrophilic Aromatic Substitution (SREAr) on Phenols
  作者：Istvan Pallagi、Andras Toro、Odon Farkas

  DOI：10.1021/jo00101a013

  日期：1994.11

  Different products are formed, depending on the para substituent (R) when 2,6-dichlorobenzoquinone N-chloroimine (1b) reacts with the anion of the 4-substituted phenol (2). If the group R can leave as a cation (i.e., R is an electrofugal leaving group) such as H, CH(2)NMe(2), CH2OH, etc., then the reaction yields indophenol (3), the normal Gibbs product. If the group R cannot leave as a cation such as CH3, the final product of the reaction will be type 10, 1,1-disubstituted 2,5-cyclohexadienone. If the group R is OH or NH2, then the reaction gives the corresponding benzoquinone 4 or benzoquinone imine 1 and 2,6-dichlorobenzoquinone imine (1d). In all these cases the reaction proceeds at a 1:1 stoichiometry. If, however, the group R can leave as an anion (i.e., R is nucleofugal leaving group) such as halogen, alkoxy, or OCH(2)Ph, then the reaction proceeds at a 1:2 stoichiometry. In this case the reaction of a second mole of phenolate with type 26 intermediate yields the indophenol product 3 and the oxidized product of the phenol. If the two ortho positions of the phenolate are substituted then the oxidized product of the phenol will be the corresponding benzoquinone. The mechanism of the reaction has been studied by kinetic and nonkinetic (NMR) methods. It has been concluded that the first step of the mechanism is a single electron transfer (SET) from the phenolate to the benzoquinone N-chloroimine 1b which is the rate-determining process in most of the cases. In some of the nucleofugal cases the final oxidation, involving the second mole of phenolate, is the rate-determining step. For the radical reaction three different alternatives are suggested: a combination of radicals in a solvent cage (direct reaction) and two different chain reactions (chain A and chain B). Quantum chemical calculations revealed that the direct reaction and the chain A mechanisms were energetically more favored than chain B. The reaction shows an extremely large para selectivity although the substitution does follow a radical mechanism.
• FUJITANI, TSUYOSHI, YUKAGAKU, 39,(1990) N, S. 380-384
  作者：FUJITANI, TSUYOSHI

  DOI：——

  日期：——
• Kurechi, Tsutao; Kato, Tetsuta, Chemical and pharmaceutical bulletin, 1983, vol. 31, # 5, p. 1772 - 1776
  作者：Kurechi, Tsutao、Kato, Tetsuta

  DOI：——

  日期：——