Sebastian Steiner, Ulli Blumenschein, Zurwa M. Shafiq, Christoph Jessen, Alexander Nitzer, Christoph Taeschler, Andreas J. Kornath
{"title":"Ring Opening of Diketene in Superacidic Media","authors":"Sebastian Steiner, Ulli Blumenschein, Zurwa M. Shafiq, Christoph Jessen, Alexander Nitzer, Christoph Taeschler, Andreas J. Kornath","doi":"10.1021/acs.joc.4c02601","DOIUrl":null,"url":null,"abstract":"The reactions of diketene were investigated in the HF/MF<sub>5</sub> and DF/MF<sub>5</sub> (M = As or Sb) binary superacidic systems. Depending on the stoichiometric ratio of the Lewis acids and diketene, monoprotonated acetoacetyl fluoride and diprotonated acetoacetyl fluoride were obtained. The salts were characterized by low-temperature vibrational spectroscopy, nuclear magnetic resonance spectroscopy, and single-crystal X-ray diffraction. [CH<sub>3</sub>C(OH)CH<sub>2</sub>COF][SbF<sub>6</sub>]·HF crystallizes in monoclinic space group <i>P</i>2<sub>1</sub>/<i>n</i> with four formula units per unit cell, and [CH<sub>3</sub>C(OH)CH<sub>2</sub>C(OH)F][SbF<sub>6</sub>]<sub>2</sub>·HF in triclinic space group <i>P</i><span>1</span> with two formula units per unit cell. Ring opening is discussed together with quantum chemical p<i>K</i><sub>a</sub> calculations. Monoprotonated acetoacetyl fluoride is characterized by a six-membered ring-like structure containing an intramolecular hydrogen bond, whereas the diprotonated species constitutes a 1,3-gitonic superelectrophile.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"247 1","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.4c02601","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
The reactions of diketene were investigated in the HF/MF5 and DF/MF5 (M = As or Sb) binary superacidic systems. Depending on the stoichiometric ratio of the Lewis acids and diketene, monoprotonated acetoacetyl fluoride and diprotonated acetoacetyl fluoride were obtained. The salts were characterized by low-temperature vibrational spectroscopy, nuclear magnetic resonance spectroscopy, and single-crystal X-ray diffraction. [CH3C(OH)CH2COF][SbF6]·HF crystallizes in monoclinic space group P21/n with four formula units per unit cell, and [CH3C(OH)CH2C(OH)F][SbF6]2·HF in triclinic space group P1 with two formula units per unit cell. Ring opening is discussed together with quantum chemical pKa calculations. Monoprotonated acetoacetyl fluoride is characterized by a six-membered ring-like structure containing an intramolecular hydrogen bond, whereas the diprotonated species constitutes a 1,3-gitonic superelectrophile.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.