N-(4-fluoro)benzoyl sarcosine methyl ester | 1156935-05-5

• 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: N-(4-fluoro)benzoyl sarcosine methyl ester
• 英文别名: Methyl 2-[(4-fluorobenzoyl)-methylamino]acetate
• CAS: 1156935-05-5
• 化学式: C₁₁H₁₂FNO₃
• mdl: MFCD12144405
• 分子量: 225.22
• InChiKey: MNQMAHVXEJWXRQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.272
• 拓扑面积：
  46.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  对氟苯甲醇 在 叔丁基过氧化氢 、 Iron(III) nitrate nonahydrate 、 2,2,6,6-四甲基哌啶氧化物 、 calcium carbonate 作用下， 以 水 、 乙腈 为溶剂， 反应 18.0h， 生成 N-(4-fluoro)benzoyl sarcosine methyl ester
  参考文献：
  名称：

  Tandem oxidative amidation of benzyl alcohols with amine hydrochloride salts catalysed by iron nitrate

  摘要：

  A tandem process for the oxidative amidation of benzyl alcohols with amine hydrochloride salts has been developed using inexpensive Fe(NO3)(3) as the catalyst, air and aqueous t-butyl hydroperoxide as oxidants. A wide range of benzamides have been synthesized under mild conditions. This greener amide formation method provides an economical and practical assess to benzamides from readily available and inexpensive starting materials. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2013.07.005

文献信息

• Tandem oxidative amidation of benzyl alcohols with amine hydrochloride salts catalysed by iron nitrate
  作者：Subhash Chandra Ghosh、Joyce S.Y. Ngiam、Abdul M. Seayad、Dang Thanh Tuan、Charles W. Johannes、Anqi Chen

  DOI：10.1016/j.tetlet.2013.07.005

  日期：2013.9

  A tandem process for the oxidative amidation of benzyl alcohols with amine hydrochloride salts has been developed using inexpensive Fe(NO3)(3) as the catalyst, air and aqueous t-butyl hydroperoxide as oxidants. A wide range of benzamides have been synthesized under mild conditions. This greener amide formation method provides an economical and practical assess to benzamides from readily available and inexpensive starting materials. (C) 2013 Elsevier Ltd. All rights reserved.