CAS: 65411-49-6; Tetrabutylammonium Methanesulfonate

该化合物是一种四硝基铵盐,其特点是四丁基聚氨酯和甲烷硫酸阴离子,通常是一种白色的,白色的,可溶于水和乙醇等极地溶剂的脱白固体,在各种应用中,包括作为有机合成的分阶段转移催化剂,都有用;该化合物具有良好的热稳定性,并且不挥发性,在化学工艺中提高了它的效用;其结构允许有机溶剂中溶解离子化合物,便利了否则难以作出反应;此外,四丁基聚氨甲烷硫酸盐因其毒性低而闻名,在实验室和工业环境中成为更安全的替代品;它经常用于电子化学和各种有机化合物合成中的试剂;建议适当处理和储存,以保持其应用的稳定性和有效性.

结构式图片

相似化合物

2472-88-0 32503-27-8 32503-27-8

上下游产品

CAS号616-42-2 亚硫酸二甲酯 | CAS号1643-19-2 四丁基溴化铵 | CAS号75-75-2 甲基磺酸 | CAS号10534-59-5 四丁基醋酸铵 | CAS号3570-58-9 甲磺酸2-氯乙酯 | CAS号107-06-2 1,2-二氯乙烷 | CAS号544-10-5 氯(代)正己烷 | CAS号16156-50-6 甲磺酸己酯 | CAS号24590-49-6 1-hydroxypropan... | CAS号113391-95-0 2-Hydroxy-1-pro... | CAS号822-86-6 反式-1,2-二氯环己烷 | CAS号90331-51-4 Cyclohexanol, 2... | CAS号66-27-3 甲基磺酸甲酯 | CAS号7429-37-0 (±)-反-1,2-二溴环己烷

合成工艺路线路线简述

  • 合成目标产物 Tetrabutylammonium Methanesulfonate 主要起始原料 Dimethyl Sulfite And Tetrabutylammonium Bromide
  • (文献来源)合成步骤主要原料 Dimethyl Sulfite 和 Tetrabutylammonium Bromide
📜亚硫酸二甲酯,四丁基溴化铵 110.0~115.0 °C,150.0 Kpa 条件下,反应 96.0H,以100%的收率获得产物甲基磺酸四丁基铵
参考文献:Process For The Preparation Of Onium Alkylsulfonates
标题:Process For The Preparation Of Onium Alkylsulfonates
摘要:该发明涉及一种通过在50至170oc温度下将一个铵盐卤化物或羧酸盐与对称取代的二烷基亚磺酸酯或不对称取代的二烷基亚磺酸酯反应制备亚磺酸铵盐的方法.

海关参考信息

专利信息


专利号:US-4334079-A
优先权日:1980-11-03
标 题:Synthesis of substituted benzyl esters
发明人:GREENE JAMES M; BUNNELL CHARLES A
权利人:LILLY CO ELI
摘要:A process for preparing certain substituted benzyl esters of phenylacetic acids by esterification in a solvent in which the salt of the acid is insoluble, and in the presence of a phase transfer catalyst.

专利号:US-4950368-A
优先权日:1989-04-10
标 题 :Method for paired electrochemical synthesis with simultaneous production of ethylene glycol
发明人:WEINBERG NORMAN L; GENDERS JOHN D; MAZUR DUANE J
权利人:ELECTROSYNTHESIS CO INC; SKA ASS
摘要:Paired electrochemical synthesis reactions in which ethylene glycol is formed at the cathode of a membrane divided cell at high concentrations and current efficiencies, up to 99 percent. Simultaneously, a compatible process is also conducted at the anode of the same electrochemical cell by reacting indirectly generated anode products with organic substrates to form secondary products, such as polybasic acids. The process is especially advantageous in that such secondary products, where appropriate can be further reacted with the ethylene glycol prepared from the catholyte of the same cell to form useful tertiary products, especially polyesters like polyethylene terephthalate. Mole ratios of ethylene glycol and polybasic acid can be controlled through selective use of regeneratable redox reactant.

专利号:US-9505799-B2
优先权日:2011-05-13
标题:18F-labeled precursor of PET radioactive medical supplies, and preparation method thereof
发明人:CHI DAE-YOON; LEE BYOUNG-SE; PARK CHANSOO; LEE MIN-HYUNG; CHA HYOJIN; CHO WOOJIN; KANG HEEWON; KIM KYUNGHUN
权利人:CHI DAE-YOON; LEE BYOUNG-SE; PARK CHANSOO; LEE MIN-HYUNG; CHA HYOJIN; CHO WOOJIN; KANG HEEWON; KIM KYUNGHUN; FUTURECHEM CO LTD
摘要:The present invention relates to a precursor of positron emission tomography (PET) radioactive medical supplies, a preparation method thereof, and an application thereof, and more specifically, to a precursor having a tetravalent organic salt leaving group, a preparation method, and a method for preparing desired PET radioactive medical supplies in a high radiochemical yield within a short preparation time by introducing 18 F using the same through a single step. The precursor having a tetravalent organic salt leaving group of the present invention can simplify the known complex multistep preparation of radioactive medical supplies into a single step, can save production costs because an excessive amount of a phase transfer catalyst is not required, facilitates separation of a compound after reaction, and enables rapid reaction velocity. The features are appropriate for the mass production of PET radioactive medical supplies by an automated synthesis system.

专利号:CN-115087647-A
优先权日:2018-12-07
标 题:For the preparation of 4-(2-Chloro-4-methoxy-5-methylphenyl)-N-[(1S)-2-cyclopropyl-1-(3-fluoro-4-methylphenyl) ) ethyl]-5-methyl-N-prop-2-ynyl-1,3-thiazol-2-amine synthesis method

专利号:EP-0392370-A2
优先权日:1989-04-10
标 题 :Method for paired electrochemical synthesis with simultaneous production of ethylene glycol

专利号:CA-2014055-A1
优先权日:1989-04-10
标题 :Methods for paired electrochemical synthesis with simultaneous production of ethylene glycol

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📌 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:Sokolovs, I.; Suna, E., Science of Synthesis: Hypervalent Halogens in Organic Synthesis, (2025) .
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