CAS: 2050-07-9; 4-Methyl-1-Phenylpentan-1-One

该化合物是分子式C12H16O的有机化合物,其特征为氯酮功能组,其特征为碳基(C=O)组与碳原子结合,该化合物一般是无色的,淡黄色的,有甜美味的液体,在乙醇和乙醚等有机溶剂中可溶解,但水溶性有限,该化合物主要用作有机合成的中间体以及各种香料和调味剂的生产.此外,该化合物在制药和其他化学产品的制造中也有应用.由于其化学结构,4-甲基-1-苯基-1-苯基-苯并酮的化学结构可能具有中度毒性,在处理时应采取适当安全措施.与许多有机化合物一样,重要的是考虑其环境影响和在不同管辖区的监管地位.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

苯丙酮 1-Phenyl-Propan-1-One 93-55-0
3-氯代苯丙酮 3-Chloropropiophenone 936-59-4
苯乙酮 Acetophenone 98-86-2

合成工艺路线路线简述

  • 合成目标产物 4-Methyl-1-Phenylpentan-1-One 主要起始原料 Isopentylmagnesium Bromide Solution 2 In Diethyl Ether And Benzoyl Chloride
  • (文献来源)合成步骤主要原料 Isopentylmagnesium Bromide Solution 2 In Diethyl Ether 和 Benzoyl Chloride
📜Magnesium,2-Methylbutane,Bromide置于oxidizing Agent体系中,用 四氢呋喃,二氯甲烷 用作溶剂,化学反应生成4-甲基-1-苯基戊烷-1-酮
参考文献:远程未激活的c(sp3)-H键的区域选择性乙烯基化:访问复杂的氟烷基化烯烃.
标题:远程未激活的c(sp3)-H键的区域选择性乙烯基化:访问复杂的氟烷基化烯烃.
摘要:通过直接活化未反应的ch键将特定的官能团区域选择性地引入脂族位置具有很大的合成价值.尽管通过氢原子转移过程在自由基介导的c(sp 3)-H键的官能化方面取得了进展,但远端c(sp 3)-H键的位点选择性乙烯基化仍处于探索中.本文报道的是一种新的协议,用于未激活的c(sp 3)-H键的区域选择性乙烯基化.远程c(sp 3)-H活化是由以c为中心的自由基而不是常用的n和o自由基促进的.该反应具有很高的产物多样性和合成效率,提供了大量合成有价值的e 带有三/二/单氟甲基和全氟烷基的烯烃
Doi:10.1002/anie.201812927

海关参考信息

专利信息


专利号:US-6465693-B2
优先权日:1998-02-26
标 题 :Metal-catalyzed arylations of hydrazines, hydrazones, and related substrates
发明人:BUCHWALD STEPHEN L; WAGAW SEBLE; GEIS O
权利人:MASSACHUSETTS INST TECHNOLOGY
摘要:A method is provided for the transition metal-catalyzed arylation, or vinylation, of hydrazines, hydrazones, and the like. Additionally, the invention provides a conceptually novel strategy, the cornerstone of which is the transition metal-catalyzed arylation or vinylation method, for the synthesis of indoles, carbazoles, and the like. The methods and strategies of the invention may be utilized in standard, parallel, and combinatorial synthetic protocols.

专利号:US-5936128-A
优先权日:1993-11-19
标题:5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents
发明人:ELLSWORTH EDMUND LEE; LUNNEY ELIZABETH; TAIT BRADLEY DEAN
权利人:WARNER LAMBERT CO
摘要:The present invention relates to novel 5,6-dihydropyrone derivatives and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The 5,6-dihydropyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized 5,6-dihydropyrones and of related structures.

专利号:WO-2007044270-A1
优先权日:2005-10-06
标 题:Process for producing high purity ketones by friedel-crafts acylation at low temperature
发明人:MANIMARAN THANIKAVELU; HARKINS ALVIN E
权利人:ALBEMARLE CORP; MANIMARAN THANIKAVELU; HARKINS ALVIN E
摘要:The present invention relates to improved conditions for the Friedel-Crafts acylation of alkylbenzenes and to application of these improved conditions to the synthesis of para-isobutyl acetophenone and ibuprofen. The reaction conditions include operating the reaction at a temperature below 0°C and typically below -10° C.

专利号:US-5840751-A
优先权日:1993-11-19
标题 :5,6-dihydropyrone derivatives as protease inhibitors and antiviral agents
发明人:ELLSWORTH EDMUND LEE; LUNNEY ELIZABETH; TAIT BRADLEY DEAN
权利人:WARNER LAMBERT CO
摘要:The present invention relates to novel 5,6-dihydropyrone derivatives and related structures which potently inhibit the HIV aspartyl protease blocking HIV infectivity. The 5,6-dihydropyrone derivatives are useful in the development of therapies for the treatment of bacterial and viral infections and diseases, including AIDS. The present invention is also directed to methods of synthesis of multifunctionalized 5,6-dihydropyrones and of related structures.

专利号:US-5723708-A
优先权日:1994-09-29
标 题 :Method for producing cyclopentadienes
发明人:MATSUMURA YASUO; SUYAMA KAZUHARU; INOMATA YOSHIHISA
权利人:NIPPON PETROCHEMICALS CO LTD
摘要:A method for producing cyclopentadienes which comprises the step of cyclodehydration of an unsaturated carbonyl compound having a specific chemical structure in a vapor phase in the presence of a specific solid acid catalyst. The cyclopentadienes of the invention can be produced in a high yield from inexpensive starting materials through a simplified reaction process and are useful as intermediate compounds for organic synthesis.

专利号:CN-102516062-A
优先权日:2011-12-02
标题:A kind of Friedel-Crafts reaction solution hydrolysis external circulation heat exchange process and device for ibuprofen synthesis

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

合成参考文献


摘要:Collier, S. J., Science of Synthesis, (2007) 33, 483.
摘要:Friestad, G. K., Science of Synthesis, (2009) 40, 317.
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