4-(N,N-二乙氨甲酰基)苯硼酸 | 389621-80-1

• 物质功能分类: 化学试剂 - 有机试剂 - 硼酸酯
• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 4-(N,N-二乙氨甲酰基)苯硼酸
• 中文别名: 4-(二乙基氨甲酰基)苯硼酸；4-二甲酰基苯硼酸；4-(二乙基氨基甲酰)苯硼酸；4-(N,N-二乙基氨甲酰基)苯硼酸；4-(N,N)-二乙酰胺基苯硼酸
• 英文名称: 4-(N,N-diethylaminocarbonyl)phenylboronic acid
• 英文别名: 4-[(diethylamino)carbonyl]phenylboronic acid；4-(diethylamino)carbonylphenylboronic acid；(4-(diethylcarbamoyl)phenyl)boronic acid；[4-(diethylcarbamoyl)phenyl]boronic acid；4-(N,N-diethylaminocarbonyl)phenyl boronic acid；{4-[(diethylamino)carbonyl]phenyl}boronic acid
• CAS: 389621-80-1
• 化学式: C₁₁H₁₆BNO₃
• mdl: MFCD03411949
• 分子量: 221.064
• InChiKey: ZCGVBHIMRVYWOH-UHFFFAOYSA-N

物化性质

• 熔点：
  138-142°C
• 沸点：
  423.3±47.0 °C(Predicted)
• 密度：
  1.14±0.1 g/cm3(Predicted)
• 溶解度：
  溶于甲醇

计算性质

• 辛醇/水分配系数(LogP)：
  1.47
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.363
• 拓扑面积：
  60.8
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 危险等级：
  IRRITANT
• 危险品标志：
  Xi
• 安全说明：
  S26,S36/37/39
• 危险类别码：
  R36/37/38
• 海关编码：
  2931900090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H315,H319,H335

SDS

Material Safety Data Sheet

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Section 1. Identification of the substance
4-(N,N-Diethylaminocarbonyl)phenylboronic acid
Product Name:
Synonyms: N,N-Diethyl 4-boronobenzamide

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Section 2. Hazards identification
Harmful by inhalation, in contact with skin, and if swallowed.
H315: Causes skin irritation
H319: Causes serious eye irritation
H335: May cause respiratory irritation
P261: Avoid breathing dust/fume/gas/mist/vapours/spray
Wear protective gloves/protective clothing/eye protection/face protection
P280:
P305+P351+P338: IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present
and easy to do – continue rinsing
P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing
P405: Store locked up

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Section 3. Composition/information on ingredients.
4-(N,N-Diethylaminocarbonyl)phenylboronic acid
Ingredient name:
CAS number: 389621-80-1

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Section 4. First aid measures
Immediately wash skin with copious amounts of water for at least 15 minutes while removing
Skin contact:
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.
Wash out mouth with copious amounts of water for at least 15 minutes. Seek medical attention.
Ingestion:

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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.

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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.

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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.
Storage: Store in closed vessels.

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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.

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Section 9. Physical and chemical properties
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C11H16BNO3
Molecular weight: 221.1

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

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Section 11. Toxicological information
No data.

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Section 12. Ecological information
No data.

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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.

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

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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.

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SECTION 16 - ADDITIONAL INFORMATION
N/A

反应信息

• 作为反应物：
  描述：

  4-(N,N-二乙氨甲酰基)苯硼酸 在 tert-butylammonium hexafluorophosphate(V) 、 N,N'-dimethyl-4,4'-bipyridinium dihexafluorophosphate 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以82%的产率得到N,N-二乙基-4-羟基苯甲酰胺
  参考文献：
  名称：

  Metal-Free Electrocatalytic Aerobic Hydroxylation of Arylboronic Acids

  摘要：

  Hydroxylation of arylboronic acids to aryl alcohols was realized by a scalable electrocatalytic method. The present electrochemical hydroxylation employs low-cost methyl viologen as an organic cathodic electrocatalyst and involves O-2 as a green and sustainable reactant. The electrocheinical kinetic studies shown here can be a powerful tool to gain rich mechanistic and kinetic information and thus an in-depth understanding of the electrocatalytic mechanism.

  DOI：

  10.1021/acs.orglett.7b02483
• 作为产物：
  描述：

  4-羧基苯硼酸 、 二乙胺 在 N,N-diethanolaminomethyl polystyrene 、 水 、 1-羟基苯并三唑 、 N,N'-二异丙基碳二亚胺 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 19.02h， 以59%的产率得到4-(N,N-二乙氨甲酰基)苯硼酸
  参考文献：
  名称：

  通用固相方法用于硼酸的固定化，衍生化和树脂到树脂的转移反应。

  摘要：

  含硼酸的分子广泛用于生物学，医学和合成领域。然而，这些化合物往往难以通过溶液相方法处理。在此，该问题通过用于官能化硼酸的衍生化的第一种通用固相方法的开发来解决。该方法基于使用二乙醇胺树脂锚，该锚通过避免在酯化过程中彻底去除水的需要而促进了硼酸的固定。通过在室温下在无水溶剂中简单搅拌，可以在数分钟内将多种硼酸固定在N，N-二乙醇氨基甲基聚苯乙烯（DEAM-PS，1）上。通过（1）DEAM-PS负载的对甲苯基硼酸的（1）NMR分析显示了形成具有假定的NB配位的双环二乙醇胺硼酸酯的证据。通过紫外光谱研究了DEAM-PS树脂对相同型号硼酸的水解裂解。水解和附着显示在快速达到的平衡下发生，并且需要大量过量的水（> 32当量）以实现从DEAM-PS实际定量释放硼酸。尽管它们对水和醇具有相对的敏感性，但可以用甲酰基，溴甲基，羧基或氨基官能化的DEAM-PS结合的芳基硼酸以良好或极高的收率转化成各种胺，酰

  DOI：

  10.1021/jo0106501
• 作为试剂：
  描述：

  tert-butyl 5-(methoxymethoxy)-4-(trifluoromethylsulfonyloxy)spiro[chromene-2,4'-piperidine]-1'-carboxylate 、 4-(N,N-二乙氨甲酰基)苯硼酸 在 4-(N,N-二乙氨甲酰基)苯硼酸 作用下， 以62的产率得到tert-butyl 4-(4-(diethylcarbamoyl)phenyl)-5-(methoxymethoxy)spiro[chromene-2,4'-piperidine]-1'-carboxylate
  参考文献：
  名称：

  J. Med. Chem. 2008, 51, 5893-5896

  摘要：

  DOI：

文献信息

• Shuttle arylation by Rh(I) catalyzed reversible carbon–carbon bond activation of unstrained alcohols
  作者：Marius D.R. Lutz、Valentina C.M. Gasser、Bill Morandi

  DOI：10.1016/j.chempr.2021.02.029

  日期：2021.4

  transfer hydrogenation and borrowing hydrogen reactions paved the way to manipulate simple alcohols in previously unthinkable manners and circumvented the need for hydrogen gas. Analogously, transfer hydrocarbylation could greatly increase the versatility of tertiary alcohols. However, this reaction remains unexplored because of the challenges associated with the catalytic cleavage of unactivated C–C bonds

  转移氢化和借用氢反应的出现为以以前无法想象的方式操作简单的醇铺平了道路，并避免了对氢气的需求。类似地，转移烃基化可以大大提高叔醇的多功能性。然而，由于与未活化的CC键的催化裂解有关的挑战，该反应仍未得到探索。在本文中，我们报道了铑（I）催化的穿梭芳基化反应，通过氧化还原中性β-碳消除机制，在未应变的三芳基醇中裂解C（sp 2）-C（sp 3）键。使用良性醇作为潜在的C，实现了从叔醇到酮的取代（杂）芳基的选择性转移烃基化-亲核试剂。所有初步的机械实验都支持可逆的β-碳消除/迁移插入机制。在更广泛的背景下，这种新颖的反应性为催化叔醇的操作提供了新的平台。
• Transforming Benzylic Amines into Diarylmethanes: Cross-Couplings of Benzylic Pyridinium Salts via C–N Bond Activation
  作者：Jennie Liao、Weiye Guan、Brian P. Boscoe、Joseph W. Tucker、John W. Tomlin、Michelle R. Garnsey、Mary P. Watson

  DOI：10.1021/acs.orglett.8b01062

  日期：2018.5.18

  nickel-catalyzed cross-coupling of benzylic pyridinium salts with arylboronic acids was developed. Coupled with chemoselective pyridinium formation, this method allows benzyl primary amines to be efficiently converted to di(hetero)arylmethanes. Excellent heteroaryl and functional group tolerance is observed, and a one-pot procedure enables benzylic amines to be converted to diarylmethanes directly.

  开发了镍催化的苄基吡啶鎓盐与芳基硼酸的交叉偶联。结合化学选择性吡啶鎓的形成，该方法可使苄基伯胺有效地转化为二（杂）芳基甲烷。观察到优异的杂芳基和官能团耐受性，一锅法可使苄基胺直接转化为二芳基甲烷。
• Compounds and methods for inhibiting the interaction of BCL proteins with binding partners
  申请人：Castro C. Alfredo

  公开号：US20060025460A1

  公开（公告）日：2006-02-02

  One aspect of the present invention relates to heterocyclic compounds that bind to bcl proteins and inhibit Bcl function. Another aspect of the present invention relates to compositions comprising a heterocyclic compound of the invention. The present invention provides methods for treating and modulating disorders associated with hyperproliferation, such as cancer.

  本发明的一个方面涉及结合到bcl蛋白并抑制Bcl功能的杂环化合物。本发明的另一个方面涉及包含本发明的杂环化合物的组合物。本发明提供了用于治疗和调节与过度增殖相关的疾病，如癌症的方法。
• [EN] CATECHOL O-METHYLTRANSFERASE ACTIVITY INHIBITING COMPOUNDS<br/>[FR] COMPOSÉS INHIBANT L'ACTIVITÉ DE LA CATÉCHOL O-MÉTHYLTRANSFÉRASE
  申请人：ORION CORP

  公开号：WO2013175053A1

  公开（公告）日：2013-11-28

  Compounds of formula (I), wherein R1 is as defined in the claims, exhibit COMT enzyme inhibiting activity and are thus useful as COMT inhibitors.

  式（I）中的化合物，其中R1如权利要求中定义的，具有COMT酶抑制活性，因此可用作COMT抑制剂。
• Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C–N Bond Activation
  作者：Corey H. Basch、Jennie Liao、Jianyu Xu、Jacob J. Piane、Mary P. Watson

  DOI：10.1021/jacs.7b02389

  日期：2017.4.19

  strategy to harness alkyl amines as alkylating agents via C-N bond activation. This Suzuki-Miyaura cross coupling of alkylpyridinium salts, readily formed from primary amines, is the first example of a metal-catalyzed cross coupling via C-N bond activation of an amine with an unactivated alkyl group. This reaction enjoys broad scope and functional group tolerance. Primary and secondary alkyl groups can be

  我们开发了一种通过 CN 键活化利用烷基胺作为烷化剂的策略。这种烷基吡啶盐的 Suzuki-Miyaura 交叉偶联很容易由伯胺形成，是金属催化交叉偶联的第一个例子，通过 CN 键活化胺与未活化的烷基。该反应具有广泛的范围和官能团耐受性。可以安装伯和仲烷基。初步研究表明 NiI/NiIII 催化循环。