O-methyl 4-methylbenzenecarbothioate | 5977-80-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: O-methyl 4-methylbenzenecarbothioate
• 英文别名: 4-Methyl-thiobenzoesaeure-O-methylester；p-Methyl-thiobenzoesaeure-O-methylester；4-Methylthiobenzoic acid methyl ester
• CAS: 5977-80-0
• 化学式: C₉H₁₀OS
• 分子量: 166.244
• InChiKey: QDCGALYJVNRRBA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  41.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  O-methyl 4-methylbenzenecarbothioate 以52%的产率得到ethyl 5-(p-tolyl)thiazole-4-carboxylate
  参考文献：
  名称：

  Compounds for treating and preventing cognitive diseases and depression

  摘要：

  公开了具有单胺氧化酶抑制性能且具有低毒性的乙二胺单酰胺化合物，其化学式为R--CO--NH--CH.sub.2 --CH.sub.2 --NH.sub.2，其中R是下列基团之一：##STR1## 其中R.sup.1为苯基、单卤苯基、单较低烷基苯基、单较低烷氧基苯基、单三氟甲基苯基、单氰基苯基或单芳基-较低烷氧基苯基、双卤苯基、呋喃基、噻吩基或单卤噻吩基，R.sup.2为氢、卤素或氨基，R.sup.3、R.sup.5和R.sup.7各自为苯基、单卤苯基、双卤苯基、噻吩基、呋喃基或单卤呋喃基，R.sup.4和R.sup.6各自为氢或氨基，R.sup.8为氢或较低烷基，以及它们的药用可用酸盐。这些化合物具有单胺氧化酶抑制性能，低毒性，可用于治疗抑郁状态和认知障碍。

  公开号：

  US05011849A1
• 作为产物：
  描述：

  对甲基苯甲酸甲酯 在 tetraphosphorus decasulfide 作用下， 反应 1.0h， 以51%的产率得到O-methyl 4-methylbenzenecarbothioate
  参考文献：
  名称：

  2,4-二取代的5-乙酰氧基噻唑：用于合成噻唑酮和2,4,5-三取代的噻唑的有用中间体

  摘要：

  使用三步顺序，由取代的苯甲酸甲酯以中等至中等的收率制备各种2,4-二取代的5-乙酰氧基噻唑：（1）酯至硫代酸酯的转化;（2）与氨基酸的偶联;和（ 3）乙酸酐介导的环化。2，4-二取代的5-乙酰氧基噻唑的原位水解和烷基化得到相应的噻唑酮和2,4,5-三取代的噻唑。这种方法可以很容易地应用于基于噻唑的化学文库的合成。

  DOI：

  10.1016/j.tetlet.2008.03.140

文献信息

• THE PREPARATION AND REACTIONS OF UNSYMMETRICAL THIOCARBONYL DISULFIDES
  作者：Tomonori Katada、Sadaaki Tsuji、Tatsushi Sugiyama、Shinzi Kato、Masateru Mizuta

  DOI：10.1246/cl.1976.441

  日期：1976.5.5

  Unsymmetrical thiocarbonyl disulfides (3) have been easily synthesized in good yields by the reaction of piperidinium dithiocarboxylates with sulfenyl chlorides. In the reaction of these disulfides with nucleophiles (amine and metal alkoxide), both thiocarbonyl carbon and sulfenyl sulfur atom seem to be attacked by nucleophiles. By desulfurization with triphenylphosphine thiocarbonyl disulfides converted

  不对称硫代羰基二硫化物 (3) 可以通过哌啶鎓二硫代羧酸盐与亚磺酰氯的反应以良好的收率轻松合成。在这些二硫化物与亲核试剂（胺和金属醇盐）的反应中，硫代羰基碳和硫基硫原子似乎都被亲核试剂攻击。通过用三苯基膦硫代羰基二硫化物脱硫，以高产率转化为相应的二硫酯。
• <i>Se</i>-Aryl Alkane- or Arenecarboselenothioates: Synthesis and Some Reactions
  作者：Shinzi Kato、Eiji Yasui、Kiyomitsu Terashima、Hideharu Ishihara、Toshiaki Murai

  DOI：10.1246/bcsj.61.3931

  日期：1988.11

  A series of Se-aryl carboselenothioates 3 (RCSSeAr, R=alkyl, aryl) were synthesized and characterized from the reaction of bis(thioacyl) sulfides 1 with sodium areneselenolates. The thionselenolesters 3 are stable (liquid or crystals) both thermally and to moisture. Reactions of 3 with aliphatic primary and secondary amines gave the corresponding ammonium carbodithioates 8 together with diphenyl diselenide

  通过双（硫代酰基）硫化物 1 与芳烃烯醇钠的反应，合成并表征了一系列 Se-芳基碳硒硫酸酯 3（RCSSeAr，R=烷基，芳基）。硫代硒醇酯3对热和湿气都是稳定的（液体或晶体）。3 与脂肪族伯胺和仲胺反应得到相应的二硫代碳化铵 8 和联苯二硒化物 7。相反，用芳香胺或醇钠处理得到相应的硫代酰胺或 O-烷基或 O-芳基硫酯，收率良好。3 用间氯过苯甲酸氧化得到相应的硫化物 12 [RCS(O)SeAr] 和酰基芳基硒硫化物 13 [RCOSSeAr]，它们是通过将 ass 基团重排为硫代羰基硫原子而形成的。
• New Synthesis and Some Reactions of Vinyl Arenecarbodithioates. Wittig Reaction of (Triphenylphosphonio)methyl Arenecarbodithioate Iodides
  作者：Masaru Ishida、Koh-ichi Kaga、Hiroyuki Sato、Masato Yokoi、Shinzi Kato

  DOI：10.1246/bcsj.59.1403

  日期：1986.5

  Wittig reaction of new phosphonium salts, (triphenylphosphonio)methyl arenecarbodithioate iodides, with variety of aldehydes gave the corresponding vinyl arenecarbodithioates in moderate to good yields. Reaction of the vinyl dithiocarboxylate with nucleophiles such as potassium alkoxide or alkanethiolate was investigated and found to give the thioacylated products in high yields. Ab initio molecular

  新的鏻盐，（三苯基膦基）甲基芳烃碳二硫代碘化物与各种醛的 Wittig 反应以中等至良好的产率得到相应的乙烯基芳烃二硫代碳酸酯。研究了乙烯基二硫代羧酸酯与亲核试剂如醇钾或链烷硫醇的反应，发现以高产率得到硫代酰化产物。还讨论了模型化合物二硫代甲酸乙烯酯的从头算分子轨道计算。
• Synthesis of 5-(1-Alkoxyalkylidene)tetronates by Direct Condensation Reactions of Tetronates with Thionolactones and Thionoesters
  作者：Ya-Qing Huang、Xiong-Zhi Huang、Pei-Qiang Huang

  DOI：10.1021/acs.joc.0c02502

  日期：2021.2.5

  thionolactones and thionoesters as activated forms of lactones/esters that allows the direct condensation with tetronates via one-pot enolate formation, nucleophilic addition, S-methylation, and DBU-promoted elimination. The value of the method was demonstrated by the stereoselective syntheses of two natural products: 5,6-Z-fadyenolide (Z/E ratio = 6:1) and 9,10-methylenedioxy-5,6-Z-fadyenolide (Z/E

  我们报告了从内酯/酯开始的双环和单环5-（1-烷氧基亚烷基）代酸酯的两步方法。该方法的特征在于使用硫代内酯和硫代酸酯作为内酯/酯的活化形式，其允许通过一锅式烯醇化物形成，亲核加成，S-甲基化和DBU促进的消除而与四价酸酯直接缩合。该方法的价值通过两种天然产物的立体选择性合成得到证明：5,6- Z-脂肪酸（Z / E比= 6：1）和9,10-亚甲基二氧基-5,6- Z-脂肪酸（Z / E比= 9：1）。
• Group 13 metal carbochalcogenoato complexes: Synthesis, X-ray structure analysis, and reactions
  作者：Norio Nakata、Shinzi Kato、Osamu Niyomura、Masahiro Ebihara

  DOI：10.1002/hc.21445

  日期：2018.12

  AbstractA series of alkali metal tetrakis(carbochalcogenoato)‐gallates and ‐indates M[M′(EOCR)4](solv.) (M = alkali metal; M′ = Ga, In; E = S, Se) and tris(carbodithioato)aluminum, ‐gallates and ‐indates M′ (SSCR)3 (M′ = Al, Ga, In) were prepared by the reactions of alkali metal carbochalcogenate with metal trihalogenides (M′X3; M′ = Al, Ga, In; X = Cl, Br) and by those of piperidinium carbodithioates or carbodithioic and carboselenoic acids with M′X3, respectively. An X‐ray molecular structure analysis revealed that they have an acetone molecule as a crystal solvent. The reactions of the potassium complexes K[M′ (EOCR)4](H2O) (E = S, Se) with methanol and primary and secondary amines gave the corresponding methyl ester and amides in good yields, while the reactions with iodomethane and iodine gave S‐ and Se‐methyl chalcogenoesters RCOEMe (E = S, Se) in good yields. Similar reactions of the tris(carbodithioato)gallates and ‐indates led to the corresponding O‐methyl thioesters, thioamides, and S‐methyl dithioesters in moderate to good yields. Oxidation of the tetrakis‐ and tris‐derivatives with iodine afforded the corresponding diacyl dichalcogenides (RCOE)2 (E = S, Se) and di(carbothioyl) disulfides in quantitative yields. These reactions appeared to occur on the carbonyl or selenium atom of the tetrakis compounds and on the sulfide sulfur or thiocarbonyl carbon atom of the tris‐compounds, respectively. A possible mechanism for these I2‐oxidation reactions is discussed.