4-(苯基甲基)吗啉 | 10316-00-4

• 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-(苯基甲基)吗啉
• 中文别名: 4-苯甲基吗啉
• 英文名称: 4-benzyl-morpholine
• 英文别名: N-benzylmorpholine；benzylmorpholine；4-Benzylmorpholine
• CAS: 10316-00-4
• 化学式: C₁₁H₁₅NO
• mdl: MFCD00090503
• 分子量: 177.246
• InChiKey: GVWBJJLCTWNTRU-UHFFFAOYSA-N

物化性质

• 熔点：
  194°C
• 沸点：
  309.18°C (rough estimate)
• 密度：
  1.0387

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.454
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

安全信息

• 海关编码：
  2934999090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H315,H319,H335
• 储存条件：
  2-8℃

SDS

Material Safety Data Sheet

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

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

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Section 3. Composition/information on ingredients.
Ingredient name: 4-Benzylmorpholine
CAS number: 10316-00-4

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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.

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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.
Store in closed vessels.
Storage:

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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
Appearance: Not specified
Boiling point: No data
No data
Melting point:
Flash point: No data
Density: No data
Molecular formula: C11H15NO
Molecular weight: 177.2

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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-(苯基甲基)吗啉 在 甲酸 、 potassium hydroxide 、 盐酸 作用下， 以 乙醇 、 1,4-二氧六环 为溶剂， 反应 1.0h， 以90%的产率得到吗啡啉盐酸盐
  参考文献：
  名称：

  低钯负载量的催化转移加氢脱苄基作用

  摘要：

  描述了用于加氢脱苄基反应的高效催化体系。O-苄基和N-苄基保护基的裂解是在相对较短的反应时间内使用极低的钯负载量（0.02-0.3 mol％； TON高达5000）进行的。该方法可用于多种底物，包括药学上重要的前体，并显示出克级脱保护反应。转移条件以及易于制备的Pd / C催化剂是该脱苄基反应方案的关键特征。

  DOI：

  10.1002/adsc.201900686
• 作为产物：
  描述：

  4-苯甲酰吗啉 在 十二羰基三铁 作用下， 以 二丁醚 为溶剂， 反应 24.0h， 以80%的产率得到4-(苯基甲基)吗啉
  参考文献：
  名称：

  简便，铁催化的酰胺直接还原为胺

  摘要：

  当铁很热时：已经开发出第一个使用聚甲基氢硅氧烷（PMHS）将铁和仲酰胺还原成胺的通用且有效的催化方法（参见方案）。

  DOI：

  10.1002/anie.200904677

文献信息

• PYRAZOLO[1,5a]PYRIMIDINE DERIVATIVES AS IRAK4 MODULATORS
  申请人：Arora Nidhi

  公开号：US20120015962A1

  公开（公告）日：2012-01-19

  Compounds of the formula I or II: wherein X, m, Ar, R 1 and R 2 are as defined herein. The subject compounds are useful for treatment of IRAK-mediated conditions.

  式I或II的化合物： 其中X，m，Ar，R1和R2如本文所定义。所述化合物对于治疗IRAK介导的疾病是有用的。
• [EN] AMINOPYRIMIDINE DERIVATIVES AS LRRK2 MODULATORS<br/>[FR] DÉRIVÉS AMINOPYRIMIDINIQUES UTILISÉS COMME MODULATEURS DE LRRK2
  申请人：HOFFMANN LA ROCHE

  公开号：WO2013079505A1

  公开（公告）日：2013-06-06

  Compounds of the formula (I): or pharmaceutically acceptable salts thereof, wherein A, X, R1, R2, R3 and R4 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with LRRK2 receptor, such as Parkinson's disease.

  式(I)的化合物或其药用可接受的盐，其中A、X、R1、R2、R3和R4如本文所定义。还公开了制备这些化合物的方法，并将这些化合物用于治疗与LRRK2受体相关的疾病，如帕金森病。
• BIS-AROMATIC COMPOUNDS USEFUL IN THE TREATMENT OF INFLAMMATION
  申请人：Pelcman Benjamin

  公开号：US20100286215A1

  公开（公告）日：2010-11-11

  There is provided compounds of formula (I): wherein Y, ring A, D 1 , D 2 , D 3 , L 1 , Y 1 , L 2 , Y 2 , L 3 and Y 3 have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of leukotriene C 4 synthase is desired and/or required, and particularly in the treatment of a respiratory disorder and/or inflammation.

  提供了具有以下式（I）的化合物：其中Y、环A、D1、D2、D3、L1、Y1、L2、Y2、L3和Y3的含义如描述中所示，并且其药学上可接受的盐，这些化合物在治疗需要或者期望抑制白三烯C4合酶的疾病中非常有用，特别是在治疗呼吸道疾病和/或炎症方面。
• Deoxygenative hydroboration of primary, secondary, and tertiary amides: Catalyst‐free synthesis of various substituted amines
  作者：Jaeeun Yi、Hyun Tae Kim、Ashok Kumar Jaladi、Duk Keun An

  DOI：10.1002/bkcs.12438

  日期：2022.1

  less reactive functional groups under catalyst-free conditions is an interesting aspect and requires a typical protocol. Herein, we report the synthesis of various primary, secondary, and tertiary amines through hydroboration of amides using pinacolborane under catalyst-free and solvent-free conditions. The deoxygenative hydroboration of primary and secondary amides proceeded with excellent conversions

  在无催化剂条件下相对较少反应性官能团的转化是一个有趣的方面，需要一个典型的协议。在此，我们报告了在无催化剂和无溶剂条件下，使用频哪醇硼烷对酰胺进行硼氢化合成各种伯胺、仲胺和叔胺。伯酰胺和仲酰胺的脱氧硼氢化反应以优异的转化率进行。在无催化剂条件下，反应性相对较低的叔酰胺也以中等收率转化为相应的N，N-二胺，尽管作为次要产物获得了醇。
• Copper-catalyzed reductive coupling of tosylhydrazones with amines: A convenient route to α-branched amines
  作者：Abdallah Hamze、Bret Tréguier、Jean-Daniel Brion、Mouâd Alami

  DOI：10.1039/c1ob05664f

  日期：——

  A general procedure for the reductive coupling of N-tosylhydrazones with amines in the presence of Cu(acac)2 and Cs2CO3 has been developed. The protocol is very effective and chemoselective with various primary and secondary aliphatic amines, aminoalcohols as well as azole derivatives to give α-branched amines in good yields.

  已经开发出一种通用程序，在Cu(acac)2和Cs2CO3的存在下，将N-甲苯磺酰腙与各种伯胺、仲胺、氨基醇以及氮杂环衍生物还原耦合，以良好收率得到α-支链胺。该方法非常有效且化学选择性好。