344-07-0 = 832-53-1 反应条件:1.1 Reagents: Magnesium Solvents: Tetrahydrofuran; -20 °C2.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C; 0 °C 标题:Chloropentafluorobenzene 作者:Anilkumar,R.; Et Al 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2005 卷标:1 页码:1-5]
879-06-1 = 832-53-1 反应条件:1.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C -> 0 °C 标题:1-Chloro-2,3,4,5,6-Pentafluorobenzene (Cpfb) 作者:Anilkumar,R.; Et Al 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001]
363-72-4 = 832-53-1 反应条件:1.1 Reagents: Chlorosulfonic Acid; 3 H,150 °C 标题:Development Of Hdac Inhibitors Exhibiting Therapeutic Potential In T-Cell Prolymphocytic Leukemia 作者:Toutah,Krimo; Et Al 参考文献:Journal Of Medicinal Chemistry 日期:2021 卷标:64(12) 页码:8486-8509]
778-36-9 = 832-53-1 反应条件:1.1 Reagents: Thionyl Chloride 标题:Sulfur-Nitrogen Compounds. Vii. Preparation And Reactions Of Some Perfluoro Aromatic Sulfur-Nitrogen Compounds 作者:Glander,I.; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:1979 卷标:14(5) 页码:403-20]
1306747-56-7 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7 反应条件:1.1 25 H,145 - 155 °C2.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt 标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides 作者:Bredikhin,Roman A.; Et Al 参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011]
344-07-0 = 832-53-1 反应条件:1.1 Reagents: Magnesium,Sulfur Dioxide Solvents: Tetrahydrofuran1.2 Reagents: Chlorine Solvents: Tetrahydrofuran 标题:Perfluoro- And Polyfluorosulfonic Acids. Part 22. Polyfluorophenyl Pentafluorobenzenesulfonates And Their Electron-Transfer Reaction With Sodium Iodide 作者:Chen,Qing Yun; Et Al 参考文献:Journal Of The Chemical Society 日期:1991 卷标:(7) 页码:1071-5]
879-06-1 = 832-53-1 反应条件:1.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C; 0 °C 标题:Chloropentafluorobenzene 作者:Anilkumar,R.; Et Al 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2005 卷标:1 页码:1-5]
= 832-53-1 反应条件:1.1 Reagents: Potassium Fluoride2.1 Reagents: Magnesium Solvents: Tetrahydrofuran; -20 °C3.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C; 0 °C 标题:Chloropentafluorobenzene 作者:Anilkumar,R.; Et Al 参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2005 卷标:1 页码:1-5]
140200-30-2 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7 反应条件:1.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt 标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides 作者:Bredikhin,Roman A.; Et Al 参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011]
776-09-0 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7 反应条件:1.1 Reagents: Sodium Bromide Solvents: Acetonitrile; Rt; 19 H,Rt2.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt 标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides 作者:Bredikhin,Roman A.; Et Al 参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011]
832-53-1 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7 反应条件:1.1 Catalysts: Cuprous Iodide; 3 H,149 - 154 °C2.1 25 H,145 - 155 °C3.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt 标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides 作者:Bredikhin,Roman A.; Et Al 参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011
氯五氟苯置于氯磺酸体系中,用 Neat (No Solvent) 作为反应溶剂,化学反应生成 2,3,4,5,6-五氟苯磺酰氯 参考文献:Development Of Hdac Inhibitors Exhibiting Therapeutic Potential In T-Cell Prolymphocytic Leukemia 标题:Development Of Hdac Inhibitors Exhibiting Therapeutic Potential In T-Cell Prolymphocytic Leukemia 摘要: DOI:10.1021/acs.Jmedchem.1C00420
专利信息
专利号:EP-0364340-B1 优先权日:1988-10-05 标题:Method for the synthesis of sulfonyl imides 摘要:Method for the synthesis of sulfonylimidides having the formula M((RSO2)2N)y, whrein M is a metal or an ammonium radical quaternary or not, the Rs, which may be identical or similar are organic monovalent radicals, particularly hydrocarbyles and preferably perfluorohydrocarbyles, in C1 to C12, and y is the valence of M. On the one hand, a silazane component selected amongst the silazane compounds M(((R2)3Si)2N)y or the associations of a silazane derivative A((R2)3Si)2N or a fluoride M1Fz of low cross-linking energy is reacted with, on the other hand, at least one sulfonic halogenite component consisting of a sulfonyl fluoride RSO2F or in the association of a sulfonyl chloride RSO2Cl with a fluoride M1Fz, M, R and y having the above-mentionned significations, M1 being selected amongst the Ms and being optionally identical to M, z being the valence of M1 and R2 representing an alkyl in C1 to C4. The imidides obtained for which the R2 are perfluorated radicals and M is an alkaline metal such as Li are usable in association with polyethers for the production of materials of the ionic conduction type for all solid generators in thin films.
专利号:US-5256821-A 优先权日:1988-10-05 标题:Method of synthesis of sulphonylimides 发明人:ARMAND MICHEL B 权利人:ELF AQUITAINE; HYDRO QUEBEC 摘要:Method for the synthesis of sulfonylimidides having the formula M((RSO 2 ) 2 N) y , wherein M is a metal or an ammonium radical quaternary or not, the Rs, which may be identical or similar are organic monovalent radicals, particularly hydrocarbyles and preferably perfluorohydrocarbyles, in C 1 to C 12 , and y is the valence of M. On the one hand, silazane component selected amongst the silazane compounds M(((R 2 ) 3 Si) 2 N) y or the associations of a silazane derivative A((R 2 ) 3 Si) 2 N or a fluoride M 1 F z of low cross-linking energy is reacted with, on the other hand, at least one sulfonic halogenite component consisting of a sulfonyl fluoride RSO 2 F or in the association of a sulfonyl chloride RSO 2 Cl with a fluoride M 1 F z , M, R and y having the above-mentioned significations, M being selected amongst the Ms and being optionally identical to M, z being the valence of M 1 and R 2 representing an alkyl in C 1 to C 4 . The imidides obtained for which the R 2 are perfluorated radicals and M is an alkaline metal such as Li are usable in association with polyethers for the production of materials of the ionic conduction type for all solid generators in thin films.
专利号:US-2010150835-A1 优先权日:2007-02-27 标题:Synthesis of [18F] Fluoromethyl Benzene Using Benzyl Pentafluorobenzenesulfonate 发明人:LANGSTROM BENGT; KARIMI FARHAD; BLOM ELISABETH 权利人:LANGSTROM BENGT; KARIMI FARHAD; BLOM ELISABETH 摘要:The present invention discloses the reactivity of ponytail (“PTâ€?) sulfonates as leaving groups in nucleophilic fluorination reactions. The results showed that using a pentafluorobenzenesulfonate precursor is a suitable leaving group for n. c. a. nucleophilic 18 F-fluorination in synthesis of [ 18 F]fluoromethyl benzene, wherein this is a suitable leaving group for 18F-labeling with moderate reactivity. The PT-precursor seems to be quite stable. In an attempt to purify the crude 18F-labeled product using fluorous solid phase extraction (F-SPE), the radio labeled impurities decreased significantly. This provides an opportunity for utilizing PT methodology in both simple and fast purification methods.
专利号:US-5214218-A 优先权日:1992-05-04 标题 :One step synthesis of methyl t-butyl ether from t-butanol using haloacid-modified clay catalysts 发明人:KNIFTON JOHN F 权利人:TEXACO CHEMICAL 摘要:A method is disclosed wherein t-butanol is reacted with methanol in a reaction zone in one step to provide methyl tert-butyl ether and the improvement of accomplishing the reaction which comprises: n a. Using a catalyst comprising a montmorillonite clay treated with a haloacid; n b. continuously contacting said t-butanol and methanol in a molar amount of about 0.1 to 10 moles of methanol per mole of t-butanol with said catalyst at a temperature of about 20° C. to about 250° C. and a pressure of about atmospheric to about 1000 psig to obtain the methyl tert-butyl ether product.
专利号:EP-2883866-A1 优先权日:2012-08-13 标题 :INTERMEDIATE FOR SYNTHESIS OF 1-(2-DEOXY-2-FLUORO-4-THIO-beta-D-ARABINOFURANOSYL) CYTOSINE, INTERMEDIATE FOR SYNTHESIS OF THIONUCLEOSIDE, AND METHODS FOR PRODUCING THESE INTERMEDIATES
专利号:WO-2014027658-A1 优先权日:2012-08-13 标题 :INTERMEDIATE FOR SYNTHESIS OF 1-(2-DEOXY-2-FLUORO-4-THIO-β-D-ARABINOFURANOSYL) CYTOSINE, INTERMEDIATE FOR SYNTHESIS OF THIONUCLEOSIDE, AND METHODS FOR PRODUCING THESE INTERMEDIATES
[参考文献]: A Sentissi, Et Al. Pentafluorobenzenesulfonyl Chloride: A New Electrophoric Derivatizing Reagent With Application To Tyrosyl Peptide Determination By Gas Chromatography With Electron Capture Detection. Anal Chem. 1984 Nov;56(13):2512-7. [参考文献]: G B Baker, Et Al. Electron-Capture Gas Chromatographic Analysis Of Beta-Phenylethylamine In Tissues And Body Fluids Using Pentafluorobenzenesulfonyl Chloride For Derivatization. J Chromatogr. 1986 Sep 5;381(2):211-7. [参考文献]: Kay Rittenbach, Et Al. A Rapid, Sensitive Electron-Capture Gas Chromatographic Procedure For Analysis Of Metabolites Of N-Methyl,N-Propargylphenylethylamine, A Potential Neuroprotective Agent. J Pharmacol Toxicol Methods. 2005 Nov-Dec;52(3):373-8. [参考文献]: S J Asghar, Et Al. A Rapid Method Of Determining Amphetamine In Plasma Samples Using Pentafluorobenzenesulfonyl Chloride And Electron-Capture Gas Chromatography. J Pharmacol Toxicol Methods. 2001 Sep-Oct;46(2):111-5. [参考文献]: Zhao-Qian Liu, Et Al. Simultaneous Determination Of Fluoxetine And Its Metabolite P-Trifluoromethylphenol In Human Liver Microsomes Using A Gas Chromatographic-Electron-Capture Detection Procedure. J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Apr 5;769(2):305-11.
合成参考文献
摘要:Kwiatkowska, M.; Kiełbasiński, P., Science of Synthesis: Knowledge Updates, (2024) 3, 436.