2-(Phenyl-acetoxymethyl)acetanilid | 30651-46-8

• 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: 2-(Phenyl-acetoxymethyl)acetanilid
• 英文别名: o-Acetamidobenzhydrylacetat；(2-acetamidophenyl)(phenyl)methyl acetate；[(2-acetamidophenyl)-phenylmethyl] acetate
• CAS: 30651-46-8
• 化学式: C₁₇H₁₇NO₃
• 分子量: 283.327
• InChiKey: MDOPLBWDCDTHMZ-UHFFFAOYSA-N

物化性质

• 沸点：
  457.9±33.0 °C(Predicted)
• 密度：
  1.184±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  21.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  55.4
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  2-(Phenyl-acetoxymethyl)acetanilid 在 劳森试剂 作用下， 以 甲苯 为溶剂， 反应 15.0h， 以50%的产率得到2-Methyl-4-phenyl-4H-benzo[d][1,3]thiazine
  参考文献：
  名称：

  Sulfur-containing Heterocycles Derived by Reaction of N-Thioacylamino Alcohols with Lawesson’s Reagent and Saponification of N-Thioacylamino Esters

  摘要：

  The treatment of 2-N-thioacylamino alcohols (1) with Lawesson's reagent [LR: 2,4-bis(p-methoxyphenyl)-1,3,2,4-dithiaphosphetane 2,4-disulfide] afforded the sulfur-containing heterocycles, 1,3-thiazolines (2) in moderate to good yields, exclusively. The saponification of N-thioacylamino esters (4), which were prepared by the thionation of N-acylamino esters (3) with LR, with K2CO3 gave 3,1-benezothiazines (5) and 3,1-benzoxazines (6).

  DOI：

  10.3987/com-02-s(m)9
• 作为产物：
  描述：

  2-氨基二苯甲酮 在 sodium tetrahydroborate 、 三乙胺 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 1.0h， 生成 2-(Phenyl-acetoxymethyl)acetanilid
  参考文献：
  名称：

  Sunlight-Driven Forging of Amide/Ester Bonds from Three Independent Components: An Approach to Carbamates

  摘要：

  A photoredox catalytic route to carbamates enabled by visible irradiation (or simply sunlight) has been developed. This process leads to a novel approach to the construction of heterocyclic rings wherein the amide or ester motifs of carbamates were assembled from three isolated components. Large-scale experiments were realized by employing continuous flow techniques, and reuse of photocatalyst demonstrated the green and sustainable aspects of this method.

  DOI：

  10.1021/acs.orglett.6b02811

文献信息

• Enantiospecific synthesis of 5-phenylpyrrolo[2,1-c][1,4]benzodiazepines
  作者：Loreto Legerén、Eduardo Gómez、Domingo Domínguez

  DOI：10.1016/j.tetlet.2008.09.168

  日期：2008.12

  Enantiomerically pure 5-phenylpyrrolo[2,1-c][1,4]benzodiazepines were synthesized starting from 2-aminobenzophenones and 2-amino-4-methoxyxanthone, using l-proline as a chiral building block.

  使用1-脯氨酸作为手性结构单元，从2-氨基二苯甲酮和2-氨基-4-甲氧基黄酮开始合成对映体纯的5-苯基吡咯并[2,1- c ] [1,4]苯并二氮杂。
• Metanolysis of phenyl-substituted benzhydryl chlorides
  作者：Gordon W. Gribble、Michael S. Smith

  DOI：10.1021/jo00817a038

  日期：1971.9