5-氯-2-碘甲苯 | 23399-70-4

• 物质功能分类: 有机原料 - 烃类化合物及其衍生物 - 芳香烃
• 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: 5-氯-2-碘甲苯
• 中文别名: 2-碘-5-氯甲苯；5-氯-2-碘代甲苯；4-氯-1-碘-2-甲苯
• 英文名称: 4-chloro-1-iodo-2-methylbenzene
• 英文别名: 2-methyl-4-chloroiodobenzene；2-iodo-5-chlorotoluene；2-Jod-5-chlor-toluol；5-Chloro-2-iodotoluene
• CAS: 23399-70-4
• 化学式: C₇H₆ClI
• mdl: MFCD00060665
• 分子量: 252.482
• InChiKey: ZZNUQVQAJVZRKW-UHFFFAOYSA-N

物化性质

• 熔点：
  -21°C
• 沸点：
  120-122°C
• 密度：
  1.82
• 闪点：
  120-122°C/15mm
• 保留指数：
  1311.5
• 稳定性/保质期：

  如果按照规格使用和储存，则不会分解。避免接触氧化物和光线。

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  9
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

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：
  2903999090
• 危险性防范说明：
  P261,P305+P351+P338
• 危险性描述：
  H315,H319,H335
• 储存条件：
  将贮藏器密封后，放入一个紧密封闭的容器中，并将其存放在阴凉、干燥的地方。

SDS

Material Safety Data Sheet

---

Section 1. Identification of the substance
5-Chloro-2-iodotoluene
Product Name:
Synonyms: 4-Chloro-1-iodo-2-methylbenzene

---

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

---

Section 3. Composition/information on ingredients.
5-Chloro-2-iodotoluene
Ingredient name:
CAS number: 23399-70-4

---

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:

---

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.
Storage: Store in closed vessels, refrigerated.

---

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
Not specified
Appearance:
Boiling point: No data
Melting point: No data
Flash point: No data
Density: No data
Molecular formula: C7H6ClI
Molecular weight: 252.5

---

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

---

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

合成制备方法

---

用途

---

反应信息

• 作为反应物：
  描述：

  5-氯-2-碘甲苯 在 N-溴代丁二酰亚胺(NBS) 、 potassium tert-butylate 、 potassium carbonate 、 copper(II) sulfate 、 过氧化苯甲酰 作用下， 以 1,4-二氧六环 、 N,N-二甲基甲酰胺 为溶剂， 反应 9.5h， 生成 5-chloro-1-(4-chlorophenyl)-3-(phenylthio)-1H-indole
  参考文献：
  名称：

  CuSO₄-Catalyzed Tandem C(sp³)–H Insertion Cyclization of Toluenes with Isonitriles to Form Indoles

  摘要：

  A CuSO4-catalyzed tandem benzylic C-H insertion cyclization of toluene derivatives and isonitriles is described. The naturally abundant salt CuSO4 serves as a low-cost ligand-free redox catalyst. This reaction provides a practical modular synthesis of N-aryl indoles from isonitriles.

  DOI：

  10.1021/acs.orglett.9b03751
• 作为产物：
  描述：

  甲基硝基苯 在 盐酸 、 tin 作用下， 生成 5-氯-2-碘甲苯
  参考文献：
  名称：

  Beilstein; Kuhlberg, Justus Liebigs Annalen der Chemie, 1870, vol. 156, p. 72,77

  摘要：

  DOI：

文献信息

• Palladium-Catalyzed/Norbornene-Mediated CH Activation/<i>N</i>-Tosylhydrazone Insertion Reaction: A Route to Highly Functionalized Vinylarenes
  作者：Ping-Xin Zhou、Lan Zheng、Jun-Wei Ma、Yu-Ying Ye、Xue-Yuan Liu、Peng-Fei Xu、Yong-Min Liang

  DOI：10.1002/chem.201402097

  日期：2014.5.26

  A straightforward method for the synthesis of highly functionalized vinylarenes through palladium‐catalyzed, norbornene‐mediated CH activation/carbene migratory insertion is described. Extension to a one‐pot procedure is also developed. Furthermore, this method can also be used to generate polysubstituted bicyclic molecules. The reaction proceeds under mild conditions to give the products in satisfactory

  描述了一种通过钯催化，降冰片烯介导的CH活化/卡宾迁移插入合成高度官能化乙烯基芳烃的简单方法。还开发了扩展到一锅法的程序。此外，该方法也可以用于产生多取代的双环分子。反应在温和的条件下进行，使用容易获得的起始原料，以令人满意的产率得到产物。这是Catellani–Lautens反应，其中包含不同类型的偶联伙伴。此外，该反应是第一个证明将Pd催化的重氮化合物插入与Pd催化的CH活化相结合的反应。
• Palladium-Catalyzed <i>ortho</i>-C–H Glycosylation/<i>ipso</i>-Alkenylation of Aryl Iodides
  作者：Ya-Nan Ding、Wei-Yu Shi、Ce Liu、Nian Zheng、Ming Li、Yang An、Zhe Zhang、Cui-Tian Wang、Bo-Sheng Zhang、Yong-Min Liang

  DOI：10.1021/acs.joc.0c01392

  日期：2020.9.4

  This report describes the first example of palladium-catalyzed ortho-C–H glycosylation/ipso-alkenylation of aryl iodides, and the easily accessible glycosyl chlorides are used as a glycosylation reagent. The reaction is compatible with the functional groups of the substrates, and a series of C-aryl glycosides have been synthesized in good to excellent yield and with excellent diastereoselectivity.

  该报告描述了钯催化芳基碘化物邻位-C-H糖基化/ iPSo-烯基化的第一个例子，并且易于获得的糖基氯被用作糖基化试剂。该反应与底物的官能团相容，并且已经以良好至优异的产率和优异的非对映选择性合成了一系列C-芳基糖苷。发现廉价的5-降冰片烯-2-腈作为瞬时介体可以有效地促进该反应。此外，IPSO -arylation和氰化还通过战略来实现。
• Nickel-Catalyzed Trifluoromethylselenolation of Aryl Halides Using the Readily Available [Me₄N][SeCF₃] Salt
  作者：Jia-Bin Han、Tao Dong、David A. Vicic、Cheng-Pan Zhang

  DOI：10.1021/acs.orglett.7b01839

  日期：2017.7.21

  efficient method for the construction of aryl trifluoromethyl selenoethers from the corresponding aryl halides in the presence of Ni(COD)2 and an appropriate ligand is reported. Various aryl iodides, bromides, and chlorides were smoothly converted in this reaction by simply varying the ligand, which afforded aryl and heteroaryl trifluoromethyl selenoethers in good to almost quantitative yields. The reaction

  在Ni（COD）2存在下由相应的芳基卤化物构建芳基三氟甲基硒醚的便捷有效方法并报道了合适的配体。通过简单地改变配体，各种芳基碘化物，溴化物和氯化物就可以在该反应中平稳地转化，从而以良好或几乎定量的产率提供了芳基和杂芳基三氟甲基硒醚。该反应也适用于药物样分子的合成。这项工作是有关芳基氯的三氟甲基硒化的第一份报告。本发明的镍催化方法的优点包括温和的反应条件，良好的官能团耐受性，廉价的试剂，易于操作以及不使用额外的添加剂。该方案允许直接和可靠地获得三氟甲基硒化物，而三氟甲基硒化物是新药和农用化学品的潜在筛选候选物。
• Modular and Stereoselective Synthesis of C-Aryl Glycosides via Catellani Reaction
  作者：Weiwei Lv、Yanhui Chen、Si Wen、Dan Ba、Guolin Cheng

  DOI：10.1021/jacs.0c07634

  日期：2020.9.2

  In this work, we describe a Catellani-type C-H glycosylation to provide rapid access to various highly decorated α-C-(hetero)aryl glycosides in a modular and stereoselective manner (>90 examples). The termination step is flexible, which is demonstrated by ipso-Heck reaction, hydrogenation, Suzuki coupling, and Sonogashira coupling. Application of this methodology has been showcased by preparing gl

  在这项工作中，我们描述了 Catellani 型 CH 糖基化，以模块化和立体选择性的方式（> 90 个例子）提供对各种高度装饰的 α-C-（杂）芳基糖苷的快速访问。终止步骤是灵活的，这可以通过 ipso-Heck 反应、氢化、Suzuki 偶联和 Sonogashira 偶联得到证明。通过制备糖苷-药效团缀合物和达格列净类似物展示了该方法的应用。值得注意的是，本文开发的技术代表了涉及 SN1 途径的 Catellani 型烷基化的一个前所未有的例子。
• Palladium-Catalyzed C–H Amination/[2 + 3] or [2 + 4] Cyclization via C(sp³ or sp²)–H Activation
  作者：Yang An、Yuke Li、Xiao-Yan Zhang、Zhe Zhang、Xue-Ya Gou、Ya-Nan Ding、Qiao Li、Yong-Min Liang

  DOI：10.1021/acs.orglett.1c02964

  日期：2021.10.15

  This report describes a palladium-catalyzed Catellani reaction consisting of amination/[2 + 3] or [2 + 4] cyclization via a carboxylate ligand-exchange strategy. This method effectively activates ortho-substituents that avoid a second C–H palladation. The scope of substrates was broad, o-methyl-substituted iodoarenes were applied to the reaction smoothly, and o-phenyl-substituted iodoarenes can also

  本报告描述了钯催化的 Catellani 反应，该反应由通过羧酸盐配体交换策略的胺化/[2 + 3] 或 [2 + 4] 环化组成。这种方法有效地激活了避免第二次 C–H 钯化的邻位取代基。底物范围广，邻甲基取代的碘芳烃适用于反应顺利，该方法也可以得到邻苯基取代的碘芳烃。在机理方面，密度泛函理论计算证明了关键的五元芳基-降冰片烯-钯环中间体形成和C(sp 3或sp 2 )-H活化的顺序。