4-三氟甲基苯甲酰基乙酸甲酯 | 212755-76-5

• 物质功能分类: 化学试剂 - 有机试剂 - 酯类
• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: 4-三氟甲基苯甲酰基乙酸甲酯
• 中文别名: 对三氟甲基苯甲酰乙酸乙酯；4-三氟甲基苯甲酰乙酸乙酯；3-氧代-3-(4-三氟甲基苯基)丙酸甲酯
• 英文名称: methyl 3-oxo-3-(4-(trifluoromethyl)phenyl)propanoate
• 英文别名: methyl 4-(trifluoromethyl)benzoylacetate；methyl 3-oxo-3-[4-(trifluoromethyl)phenyl]propanoate
• CAS: 212755-76-5
• 化学式: C₁₁H₉F₃O₃
• mdl: MFCD00216521
• 分子量: 246.186
• InChiKey: NMJOILIYLOHXGP-UHFFFAOYSA-N

物化性质

• 熔点：
  58-61
• 沸点：
  277.4±40.0 °C(Predicted)
• 密度：
  1.3318 (estimate)
• 溶解度：
  溶于甲醇
• 稳定性/保质期：
  遵照规定使用和储存，则不会分解。

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  17
• 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：
  43.4
• 氢给体数：
  0
• 氢受体数：
  6

安全信息

• 危险等级：
  IRRITANT
• 危险品标志：
  Xi
• 安全说明：
  S24/25
• 海关编码：
  2918300090
• 危险性防范说明：
  P261,P280,P301+P312,P302+P352,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335
• 储存条件：
  存于阴凉干燥处

SDS

Material Safety Data Sheet

---

Section 1. Identification of the substance
Product Name: Methyl 4-trifluoromethylbenzoylacetate
Synonyms:

---

Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.

---

Section 3. Composition/information on ingredients.
Ingredient name: Methyl 4-trifluoromethylbenzoylacetate
CAS number: 212755-76-5

---

Section 4. First aid measures
Skin contact: Immediately wash skin with copious amounts of water for at least 15 minutes while removing
contaminated clothing and shoes. If irritation persists, seek medical attention.
Eye contact: Immediately wash skin with copious amounts of water for at least 15 minutes. Assure adequate
flushing of the eyes by separating the eyelids with fingers. If irritation persists, seek medical
attention.
Inhalation: Remove to fresh air. In severe cases or if symptoms persist, seek medical attention.
Ingestion: Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.

---

Section 5. Fire fighting measures
In the event of a fire involving this material, alone or in combination with other materials, use dry
powder or carbon dioxide extinguishers. Protective clothing and self-contained breathing apparatus
should be worn.

---

Section 6. Accidental release measures
Personal precautions: Wear suitable personal protective equipment which performs satisfactorily and meets local/state/national
standards.
Respiratory precaution: Wear approved mask/respirator
Hand precaution: Wear suitable gloves/gauntlets
Skin protection: Wear suitable protective clothing
Eye protection: Wear suitable eye protection
Methods for cleaning up: Mix with sand or similar inert absorbent material, sweep up and keep in a tightly closed container
for disposal. See section 12.
Environmental precautions: Do not allow material to enter drains or water courses.

---

Section 7. Handling and storage
Handling: This product should be handled only by, or under the close supervision of, those properly qualified
in the handling and use of potentially hazardous chemicals, who should take into account the fire,
health and chemical hazard data given on this sheet.
Store in closed vessels.
Storage:

---

Section 8. Exposure Controls / Personal protection
Engineering Controls: Use only in a chemical fume hood.
Personal protective equipment: Wear laboratory clothing, chemical-resistant gloves and safety goggles.
General hydiene measures: Wash thoroughly after handling. Wash contaminated clothing before reuse.

---

Section 9. Physical and chemical properties
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C11H9F3O3
Molecular weight: 246.2

---

Section 10. Stability and reactivity
Conditions to avoid: Heat, flames and sparks.
Materials to avoid: Oxidizing agents.
Possible hazardous combustion products: Carbon monoxide, hydrogen fluoride.

---

Section 11. Toxicological information
No data.

---

Section 12. Ecological information
No data.

---

Section 13. Disposal consideration
Arrange disposal as special waste, by licensed disposal company, in consultation with local waste
disposal authority, in accordance with national and regional regulations.

---

Section 14. Transportation information
Non-harzardous for air and ground transportation.

---

Section 15. Regulatory information
No chemicals in this material are subject to the reporting requirements of SARA Title III, Section
302, or have known CAS numbers that exceed the threshold reporting levels established by SARA
Title III, Section 313.

---

SECTION 16 - ADDITIONAL INFORMATION
N/A

制备方法与用途

应用

4-三氟甲基苯甲酰基乙酸甲酯是一种医药中间体，可以通过将1-(4-(三氟甲基)苯基)乙酮和碳酸二甲酯在一步反应中制备得到。该化合物可用于合成抗肿瘤药物。

制备

将1-(4-(三氟甲基)苯基)乙酮（15.27 g，81.22 mmol，1.00当量）、碳酸二甲酯（50 mL）以及氢化钠（5.53 g，138.25 mmol，1.70 当量，60％）加入到500 mL 三颈圆底烧瓶中。在室温（25℃）下搅拌混合物5分钟。

通过蒸发浓缩反应混合物并过滤收集得到的固体产物，并用3×50 mL H₂O洗涤。最终得到黄色固体4-三氟甲基苯甲酰基乙酸甲酯，总产率为19.28 g，收率高达96%。

反应信息

• 作为反应物：
  描述：

  4-三氟甲基苯甲酰基乙酸甲酯 在 platinum(IV) oxide 氢气 、 溶剂黄146 作用下， 以 四氢呋喃 、 异丙醇 为溶剂， 40.0 ℃ 、620.53 kPa 条件下， 反应 96.0h， 生成 methyl 3-{[(1S)-2-amino-2-oxo-1-phenylethyl]amino}-3-[4-(trifluoromethyl)phenyl]propanoate
  参考文献：
  名称：

  Highly Diastereoselective Heterogeneously Catalyzed Hydrogenation of Enamines for the Synthesis of Chiral β-Amino Acid Derivatives

  摘要：

  Pure (Z)-enamines readily prepared from beta-ketoesters and amides using (S)-phenylglycine amide were hydrogenated with very high diastereoselectivities (up to 200:1) using heterogeneous catalysis. Hydrogenolytic cleavage of the (S)-phenylglycine amide afforded the corresponding chiral beta-aminoesters and amides. The high geometrical purity of the (Z)-enamine and a simple activation procedure for the PtO2 catalyst are essential in achieving high selectivity.

  DOI：

  10.1021/ja038812t
• 作为产物：
  描述：

  4'-三氟甲基苯乙酮 、 碳酸二甲酯 在 sodium hydride 作用下， 以 甲苯 为溶剂， 以95%的产率得到4-三氟甲基苯甲酰基乙酸甲酯
  参考文献：
  名称：

  β-酮酯、β-酮酰胺和 1,3-二酮与内炔的区域选择性铑催化加成

  摘要：

  第一铑催化的区域选择性加入1,3-二羰基化合物，包括β酮酯，β - 酮酰胺和1,3-二酮，到内部炔烃配料支链的烯丙基化合物。通过应用 RhI/DPEphos/TFA 作为催化体系，脂肪族和芳香族内部甲基取代的炔烃作为合适的底物，以良好到优异的产率区域选择性地产生有价值的支链 α-烯丙基化 1,3-二羰基化合物。一个简单的基本皂化-脱羧程序提供了获得有价值的 γ,δ-不饱和酮的途径。该反应显示出广泛的官能团耐受性，并且两个反应伙伴的众多结构变化突出了该方法的合成潜力和灵活性。

  DOI：

  10.1002/ejoc.201601230
• 作为试剂：
  描述：

  4'-三氟甲基苯乙酮 、 sodium;hydride 、 碳酸二甲酯 在 水 、 4-三氟甲基苯甲酰基乙酸甲酯 作用下， 反应 0.08h， 以This resulted in 19.28 g (96%) of methyl 3-oxo-3-(4-(trifluoromethyl)phenyl)propanoate as a yellow solid的产率得到4-三氟甲基苯甲酰基乙酸甲酯
  参考文献：
  名称：

  HETEROCYCLIC COMPOUNDS FOR THE INHIBITION OF PASK

  摘要：

  本文介绍了新的杂环化合物和组合物，以及它们作为治疗疾病的药物的应用。还提供了抑制人类或动物主体中PAS激酶（PASK）活性的方法，用于治疗糖尿病等疾病。

  公开号：

  US20120277224A1

文献信息

• Synthesis of Functionalized Imidazolium Salts via Iodine-Mediated Annulations of Enamines
  作者：Biao Xia、Wenjun Chen、Qiongli Zhao、Wenquan Yu、Junbiao Chang

  DOI：10.1021/acs.orglett.9b00541

  日期：2019.4.19

  A novel annulation reaction of two enamine molecules with iodine under basic conditions to form 4-functionalized imidazolium salts has been established. In this reaction, iodine acts as both an iodinating reagent and a Lewis acid catalyst. Features of this synthetic method include facilitative preparation of substrates, no use of transition metals, mild reaction conditions, simplicity of operation

  建立了在碱性条件下两个烯胺分子与碘的新型环化反应，形成4-官能化的咪唑鎓盐。在该反应中，碘既充当碘化试剂又充当路易斯酸催化剂。这种合成方法的特点包括便于制备底物，不使用过渡金属，温和的反应条件，操作简便和克级合成。
• Nickel-Catalyzed Enantioselective Hydrogenation of β-(Acylamino)acrylates: Synthesis of Chiral β-Amino Acid Derivatives
  作者：Xiuxiu Li、Cai You、Shuailong Li、Hui Lv、Xumu Zhang

  DOI：10.1021/acs.orglett.7b02417

  日期：2017.10.6

  β-(acylamino)acrylates has been developed, affording chiral β-amino acid derivatives with excellent yields (95–99% yield) and enantioselectivities (97–99% ee). With the Ni–Binapine system, high enantioselectivities (98–99% ee) have also been obtained in the hydrogenation of Z/E isomeric mixtures of β-alkyl and β-aryl β-(acylamino)acrylates. The synthesis of chiral β-amino acid derivatives on a gram scale has also

  已经开发了镍催化的β-（酰基氨基）丙烯酸酯不对称氢化反应，提供了具有优异收率（95-99％收率）和对映选择性（97-99％ee）的手性β-氨基酸衍生物。使用Ni-Binapine系统，在氢化β-烷基和β-芳基β-（酰基氨基）丙烯酸酯的Z / E异构体混合物时，也获得了高对映选择性（98-99％ee）。在催化剂量为0.2mol％的情况下，也已经完成了克级的手性β-氨基酸衍生物的合成。
• Synthesis of 1,4-Dihydropyridines and Related Heterocycles by Iodine-Mediated Annulation Reactions of <i>N</i>-Cyclopropyl Enamines
  作者：Lanlan Wei、Manman Wang、Yifei Zhao、Yingchao Fang、Zongxiang Zhao、Biao Xia、Wenquan Yu、Junbiao Chang

  DOI：10.1021/acs.orglett.1c03859

  日期：2021.12.17

  The annulation of N-cyclopropyl enamines to produce 1,4-dihydropyridine (1,4-DHP) derivatives is described. In the presence of molecular iodine (I2), an N-cyclopropyl enamine substrate undergoes iodination, opening of the cyclopropyl ring, and annulation with a second molecule of the substrate to form the 1,4-DHP product. This reaction is amenable to gram-scale operations under mild reaction conditions

  描述了N-环丙基烯胺的环化以产生 1,4-二氢吡啶 (1,4-DHP) 衍生物。在分子碘(I 2 )存在下，N-环丙基烯胺底物经历碘化、环丙基环开环和与底物的第二分子环化以形成1,4-DHP产物。该反应可在温和的反应条件下进行克级操作，无需过渡金属。1,4-DHP 的进一步转化导致相关的吡啶和双环框架。
• Cu-Mediated Expeditious Annulation of Alkyl 3-Aminoacrylates with Aryldiazonium Salts: Access to Alkyl <i>N</i>²-Aryl 1,2,3-Triazole-carboxylates for Druglike Molecular Synthesis
  作者：Hao-Nan Liu、Hao-Qiang Cao、Chi Wai Cheung、Jun-An Ma

  DOI：10.1021/acs.orglett.0c00006

  日期：2020.2.21

  Alkyl N-aryl 1,2,3-triazole-carboxylates are important molecules or intermediates in medicinal chemistry, but the synthesis of N2-aryl counterparts remains elusive. Herein, we describe a Cu-mediated annulation reaction of alkyl 3-aminoacrylates with aryldiazonium salts, both of which are readily available substrates. Furthermore, alkyl 2-aminoacrylates are also viable substrates. Diverse alkyl N2-aryl

  N-芳基1,2,3-三唑-羧酸烷基酯是药物化学中的重要分子或中间体，但N2-芳基对应物的合成仍然难以捉摸。在本文中，我们描述了3-氨基丙烯酸烷基酯与芳基重氮盐的Cu介导的环化反应，这两种都是容易获得的底物。此外，2-氨基丙烯酸烷基酯也是可行的底物。N 2-芳基1,2,3-三唑-羧酸烷基酯及其类似物可以在温和的条件下快速制备。特别地，该方案允许人们访问碳酸酐酶抑制剂和塞来昔布的几种药物样变体。
• Iron-catalysed 1,2-acyl migration of tertiary α-azido ketones and 2-azido-1,3-dicarbonyl compounds
  作者：Tonghao Yang、Yajun Lin、Chaoqun Yang、Wei Yu

  DOI：10.1039/c9gc02085c

  日期：——

  Iron-catalysed 1,2-acyl migration of tertiary α-azido ketones and 2-azido-1,3-dicarbonyl compounds provides a simple and atom-economical approach toward enamides and isoquinolones. This paper reports two catalyst systems for these transformations which employ iron(II) complexes [Fe(dpbz)]Br2 (dpbz = 1,2-bis(diphenylphosphino)benzene) and FeBr2/Et3N, respectively. [Fe(dpbz)]Br2 was found to be highly

  铁催化的α-叠氮基酮和2-叠氮基-1,3-二羰基化合物的1,2-酰基迁移为酰胺和异喹啉酮提供了一种简单且原子经济的方法。本文报道两种催化剂体系用于这些转化其采用铁（II）配合物的[Fe（dpbz）]溴2（dpbz = 1,2-双（二苯基膦基）苯）和FeBr 2 / ET 3 N，分别。发现[Fe（dpbz）] Br 2在将2-叠氮基-2,3-二氢-1 H-茚满-1-酮转化为异喹诺酮方面非常有效。另一方面，由于Et 3的有益作用，FeBr 2 / Et 3 N的试剂组合具有更宽的催化范围N.后一种催化剂体系可使2-叠氮基-2-甲基-1,3-二羰基化合物在温和条件下以良好的收率转化为相应的酰胺。