4-propionylphenyl benzoate | 96187-97-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 缩酚酸和缩酚酸环醚类
• 英文名称: 4-propionylphenyl benzoate
• 英文别名: 1-(4-benzoyloxy-phenyl)-propan-1-one；1-(4-Benzoyloxy-phenyl)-propan-1-on；p-(benzoyloxy)propiophenone；(4-propanoylphenyl) benzoate
• CAS: 96187-97-2
• 化学式: C₁₆H₁₄O₃
• 分子量: 254.285
• InChiKey: VVHSRGDHFAASPV-UHFFFAOYSA-N

物化性质

• 熔点：
  117 °C
• 沸点：
  404.6±28.0 °C(Predicted)
• 密度：
  1.151±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  19
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  43.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  4-propionylphenyl benzoate 在 叔丁基过氧化氢 、 碘 作用下， 以 癸烷 、 二甲基亚砜 为溶剂， 反应 8.0h， 以74%的产率得到4-(2-hydroxypropanoyl)phenyl benzoate
  参考文献：
  名称：

  Iodine promoted α-hydroxylation of ketones

  摘要：

  描述了一种在无金属条件下使用亚化学计量量的碘对酮进行α-羟基化的新方法。

  DOI：

  10.1039/c5ob00684h
• 作为产物：
  描述：

  4-羟基苯丙酮 生成 4-propionylphenyl benzoate
  参考文献：
  名称：

  Effect of Low-Fat and/or Low-Energy Diets on Anthropometric Measures in Participants of the Women’s Diet Study

  摘要：

  Objective: To compare the effects of low-fat, low-energy and combination low-fat/low-energy intervention on changes in six anthropometric measures in Caucasian and African-American free-living women.Methods: The effects of dietary counseling strategies for fat and/or energy reduction were examined on anthropometric measures in 86 pre-menopausal women, average BMI of 28 kg/m(2), who participated in a 12-week intervention trial called the Women's Diet Study. The dietary goals were 1510 of energy from fat and/or 25% reduction in energy intake, relative to reported baseline intake, using a 2 x 2 factorial design. Analysis of covariance models were constructed to evaluate changes in anthropometric measures over the 12 weeks of study.Results: The biggest difference by race was in women who were relatively heavier at baseline, in which case African-American women lost significantly less weight but decreased their waist:hip ratio to a significantly greater extent than Caucasian women. With regard to the effects of diet arm, weight loss varied depending on baseline weight, and in women with higher baseline weights, the combination low-fat/low-energy diet resulted in the most weight loss (6.7 kg, p < 0.05). Decreases in the other anthropometric measures at week 12 were more uniform across diet arms and did not depend on baseline values. After controlling for previous weight history and race, the decreases in BMI, percent body fat and waist circumference after 12 weeks were statistically equivalent with the low-fat, low-energy or combination low-fat/low-energy diets. The relatively greater decreases in percent body fat and waist circumference with the combination diet versus the low-fat or low-energy diets were not statistically significant.Conclusion: The low-fat, low-energy and combination diets all resulted in similar and statistically significant decreases in BMI, percent body fat and waist circumference over 12 weeks of intervention. The extent of weight loss, however, varied depending on baseline weight, and the combination diet was the only intervention to result in significant weight loss for women who were heavier at baseline. This indicates that, although there may be an advantage for reducing dietary fat in initially heavier women, any of these counseling strategies could be effective for improving anthropometric predictors of health risks associated with overweight status. This is useful since flexibility in dietary choices may facilitate adherence to dietary counseling in some individuals.

  DOI：

  10.1080/07315724.2002.10719192

文献信息

• Iodine Promoted Regioselective α-Sulfenylation of Carbonyl Compounds using Dimethyl Sulfoxide as an Oxidant
  作者：Yogesh Siddaraju、Kandikere Ramaiah Prabhu

  DOI：10.1021/acs.orglett.6b03084

  日期：2016.12.2

  A metal-free regioselective sulfenylation of the α-CH3 group of ketones has been achieved in the presence of the α-CH2 or α-CH group using the cross dehydrogenative (CDC) strategy. Aldehydes also exhibit good selectivity forming the corresponding α-sulfenylated products. This efficient sulfenylation of ketones or aldehydes with thiones or heterocyclic thiols utilizes dimethyl sulfoxide (DMSO) as an

  的α-CH的无金属区域选择性亚磺酰3组酮已在α-CH的存在下已经实现2使用交叉脱氢（CDC）的策略或α-CH基团。醛也表现出良好的选择性，形成相应的α-亚磺酰化产物。酮或醛与硫酮或杂环硫醇的这种有效的亚硫基化利用二甲基亚砜（DMSO）在碘存在下作为氧化剂。这种生态友好的方法使用了现成的廉价I 2和DMSO。通过合成Julia–Kocienski烯烃化中间体的前体已证明了该方法的应用。
• Process for producing optically active beta-amino alcohol
  申请人：Nishiyama Akira

  公开号：US20050277791A1

  公开（公告）日：2005-12-15

  A process for easily producing an optically active β-amino alcohol useful as a pharmaceutical intermediate from an inexpensive, readily available starting material is provided. A readily available α-substituted ketone is reacted with an optically active amine to yield a diastereomer mixture of an optically active α-substituted aminoketone. One of the diastereomers is isolated optionally after the diastereomers are converted to salts with an acid. The optically active α-substituted aminoketone or a salt thereof thus isolated was stereoselectively reduced to yield an optically active β-substituted amino alcohol. The optically active β-substituted amino alcohol is subjected to hydrogenolysis to produce an optically active β-amino alcohol or a salt thereof.

  提供了一种从廉价、易得的起始材料中轻松生产有用于制药中间体的光学活性β-氨基醇的方法。将易得的α-取代酮与光学活性胺反应，得到光学活性α-取代氨基酮的对映体混合物。在对映体混合物与酸转化为盐之后，可以选择性地分离其中一种对映体。分离出的光学活性α-取代氨基酮或其盐经立体选择性还原，得到光学活性β-取代氨基醇。将光学活性β-取代氨基醇进行氢解反应，得到光学活性β-氨基醇或其盐。
• Process for producing optically active β-amino alcohol
  申请人：Kaneka Corporation

  公开号：US07408084B2

  公开（公告）日：2008-08-05

  A process for easily producing an optically active β-amino alcohol useful as a pharmaceutical intermediate from an inexpensive, readily available starting material is provided. A readily available α-substituted ketone is reacted with an optically active amine to yield a diastereomer mixture of an optically active α-substituted aminoketone. One of the diastereomers is isolated optionally after the diastereomers are converted to salts with an acid. The optically active α-substituted aminoketone or a salt thereof thus isolated was stereoselectively reduced to yield an optically active β-substituted amino alcohol. The optically active β-substituted amino alcohol is subjected to hydrogenolysis to produce an optically active β-amino alcohol or a salt thereof.

  提供一种从廉价易得的起始物质中轻松生产有用于制药中间体的光学活性β-氨基醇的方法。将易得的α-取代酮与光学活性胺反应，得到光学活性α-取代氨基酮的对映体混合物。在将对映体转化成盐酸盐后，可以选择性地分离其中的一种对映体。随后，光学活性α-取代氨基酮或其盐被立体选择性还原，得到光学活性β-取代氨基醇。最后，对光学活性β-取代氨基醇进行氢解反应，得到光学活性β-氨基醇或其盐。
• Ni(II)-Mediated Photochemical Oxidative Esterification of Aldehydes with Phenols
  作者：Lu-Lu Chai、You-Hui Zhao、David James Young、Xinhua Lu、Hong-Xi Li

  DOI：10.1021/acs.orglett.2c02560

  日期：2022.9.30

  The photopromoted, Ni-catalyzed acceptorless dehydrogenation esterification of phenols and aromatic aldehydes has been achieved in an oxidant- and external photosensitizer-free manner. This reliable and atom-economical transformation was tolerant to a wide range of functional groups and proceeded efficiently to give various aryl benzoates in moderate to high yields. Additionally, this photocatalytic

  酚和芳香醛的光促进、Ni 催化的无受体脱氢酯化反应以无氧化剂和无外部光敏剂的方式实现。这种可靠且原子经济的转化对广泛的官能团具有耐受性，并有效地进行，以中等至高产率得到各种苯甲酸芳基酯。此外，该光催化体系在采用双镍和芳香醛催化的脂肪醛和苯酚的析氢交叉偶联方面表现出高活性。
• PROCESS FOR PRODUCING OPTICALLY ACTIVE s-AMINO ALCOHOL
  申请人：KANEKA CORPORATION

  公开号：EP1512677A1

  公开（公告）日：2005-03-09

  A process for easily producing an optically active β-amino alcohol useful as a pharmaceutical intermediate from an inexpensive, readily available starting material is provided. A readily available α-substituted ketone is reacted with an optically active amine to yield a diastereomer mixture of an optically active α-substituted aminoketone. One of the diastereomers is isolated optionally after the diastereomers are converted to salts with an acid. The optically active α-substituted aminoketone or a salt thereof thus isolated was stereoselectively reduced to yield an optically active β-substituted amino alcohol. The optically active β-substituted amino alcohol is subjected to hydrogenolysis to produce an optically active β-amino alcohol or a salt thereof.

  本发明提供了一种利用廉价易得的起始原料轻松生产具有光学活性的 β-氨基醇作为药物中间体的工艺。现成的 α 取代酮与光学活性胺反应，生成光学活性 α 取代氨基酮的非对映异构体混合物。非对映异构体中的一种非对映异构体在与酸转化成盐后被分离出来。这样分离出的具有光学活性的 α-取代氨基酮或其盐经立体选择性还原后得到具有光学活性的 β-取代氨基醇。将光学活性 β-取代氨基醇进行氢解，生成光学活性 β-氨基醇或其盐。