CAS: 52190-35-9; 2-(Methylthio)Cyclohexan-1-One

该化合物是一种有机化合物,其特征为环己酮环,在第二个位置被甲基硫磷组所取代.该化合物一般是一种无色的黄色液体,其气味独特.由于环己酮结构中存在碳基类,因此有机溶剂和表现出中极性,可溶于有机溶剂,并表现出中极性.甲基乙基酮组有助于其再活动,使它成为各种化学反应,包括核阴性替代和添加物的潜在候选物.在安全方面,它与许多有机化合物一样,应该谨慎处理,因为如果吸入或摄入,它可能会对健康造成危害.其应用范围从有机合成用途到红化工业的潜在作用,由于其独特的结构特征.

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合成工艺路线路线简述

  • 合成目标产物 2-(Methylthio)Cyclohexanone 主要起始原料 1-Cyclohexenyloxytrimethylsilane And 2,5-Cyclohexadien-1-One, 4-(Acetyloxy)-2,3,5,6-Tetramethyl-4-(Methylthio)-
  • (文献来源)合成步骤主要原料 1-Cyclohexenyloxytrimethylsilane 和 2,5-Cyclohexadien-1-One, 4-(Acetyloxy)-2,3,5,6-Tetramethyl-4-(Methylthio)-
📜1,1'-联(环己烷)-1'-烯-2-胺置于正丁基锂,草酸,二异丙胺体系中,用 水 作为反应溶剂,化学反应 38.5H,反应生成 2-(甲硫基)环己酮
参考文献:Synthesis Of Enantiomerically Enriched α-Sulfenylated Ketones And Aldehydes
标题:Synthesis Of Enantiomerically Enriched α-Sulfenylated Ketones And Aldehydes
摘要:通过含有α-氢的醛和酮的亚胺与二硫化物的反应,利用金属烯胺制备α-硫代羰基化合物.以(R)-α-苯乙胺作为手性辅助剂,观测到13-51%的对映体过量.
DOI:10.1055/s-1987-27870

海关参考信息

专利信息


专利号:US-3901899-A
优先权日:1973-04-27
标题 :Synthesis of indoles from anilines and intermediates therein
发明人:GASSMAN PAUL G
权利人:UNIV OHIO STATE RES FOUND
摘要:Preparing indoles and intermediates therefor by reacting an Nhaloaniline with a Beta -carbonylic hydrocarbon sulfide to form an azasulfonium halide, reacting the azasulfonium halide with a strong base to form a thio-ether indole derivative, and then reducing the thio-ether indole, e.g. with Raney nickel, to form the indole compound. When an acetal or ketal of the Beta carbonyl hydrocarbon sulfide is used, the azasulfonium salt is treated with a base, and then with an acid to form the thio-ether indole derivative. When an Alpha -ethyl- Beta -carbonylic hydrocarbon sulfide is used, the resulting azosulfonium salt reacts with strong base to form a thio-ether indolenine derivative, which on reduction with Raney nickel or complex metal hydrides yields 3-substituted indoles. The aniline may be an aminopyridine to form an aza-indole compound in the process. The azasulfonium salts and thio-ether indole or thio-ether indolenine derivatives can be isolated and recovered from their respective reaction mixtures. The thio-ether-indole and thio-ether indolenine derivatives are useful as intermediates to make the indoles without the thio-ether group. The indoles are known compounds having a wide variety of uses, e.g., in making perfumes, dyes, amino acids, pharmaceuticals, agricultural chemicals and the like.

专利号:US-3992392-A
优先权日:1973-04-27
标题:Synthesis of indoles from anilines and intermediates therein
发明人:GASSMAN PAUL G
权利人:UNIV OHIO STATE RES FOUND
摘要:Preparing indoles and intermediates therefor by reacting an N-haloaniline with a β-carbonylic hydrocarbon sulfide to form an azasulfonium halide, reacting the azasulfonium halide with a strong base to form a thio-ether indole derivative, and then reducing the thio-ether indole, e.g. with Raney nickel, to form the indole compound. When an acetal or ketal of the β-carbonyl hydrocarbon sulfide is used, the azasulfonium salt is treated with a base, and then with an acid to form the thio-ether indole derivative. When an α-ethyl-β -carbonylic hydrocarbon sulfide is used, the resulting azosulfonium salt reacts with strong base to form a thio-ether indolenine derivative, which on reduction with Raney nickel or complex metal hydrides yields 3-substituted indoles. The aniline may be an aminopyridine to form an aza-indole compound in the process. The azasulfonium salts and thio-ether indole or thio-ether indolenine derivatives can be isolated and recovered from their respective reaction mixtures. The thio-ether-indole and thio-ether indolenine derivatives are useful as intermediates to make the indoles without the thio-ether group. The indoles are known compounds having a wide variety of uses, e.g., in making perfumes, dyes, amino acids, pharmaceuticals, agricultural chemicals and the like.

专利号:CA-1043337-A
优先权日:1973-04-27
标题 :Synthesis of indoles from anilines and intermediates therein

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✅ COA系统入驻 | 共享模式

合成参考文献


摘要:Jończyk, A.; Kowalkowska, A., Science of Synthesis, (2006) 8, 1146.
摘要:Sartori, G.; Maggi, R., Science of Synthesis, (2008) 32, 771.
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