CAS: 5000-44-2; 1-(Phenylsulfonyl)Propan-2-One

该化合物是一个有机化合物,其特点是附于一个苯环和丙酮的磺酰功能组,通常看起来像一种白色的,白色的晶状固体,该化合物因其在有机合成中的作用而闻名,特别是在形成各种衍生物和化学反应中的试剂方面.该化合物在有机溶剂中表现出中等溶解性,使其在各种应用中有用,包括制药和农用化学品.该聚苯乙烯组的存在有助于其再活动,使其能够参与核生殖器替代和其他化学变异.此外,苯磺酰氟烯可展示生物活动,尽管具体的药理特性需要进一步调查.与许多磺酰氟化合物一样,必须小心处理,因为如果浸入或吸入,可能会对健康造成危害.总的来说,苯氟化酮是一种多用途的化合物,具有重要的合成有机化学的用途.

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相似化合物

5366-49-4 1018301-96-6 343348-18-5

上下游产品

1-(phenylsulfanyl)acetone ethanol sodium benzenesulfonate chloroacetone1-(phenylsulfonyl)pentane-2,4-dione 3-Benzenesulfonyl-6-ethylsulfanyl-hexan-2-one 1-(phenylsulfonyl)-2-propanol 1-(benzenesulfonyl)-1-diazopropan-2-one

合成工艺路线路线简述

    📜((2-Bromoallyl)Sulfonyl)Benzene置于bis-Triphenylphosphine-Palladium(II) Chloride,Copper(L) Iodide,Silver Trifluoromethanesulfonate,Caesium Carbonate,三乙胺体系中,用 四氢呋喃,二氯甲烷,乙腈 作为反应溶剂,化学反应 6.0H,反应生成 苯磺酰丙酮
    参考文献:通过金催化的n-(邻炔基芳基)-N-乙烯基磺酰胺的区域选择性环异构化反应,可轻松合成1-苯并ze庚因衍生物
    标题:通过金催化的n-(邻炔基芳基)-N-乙烯基磺酰胺的区域选择性环异构化反应,可轻松合成1-苯并ze庚因衍生物
    摘要:金催化的n-(邻炔基芳基)-N-乙烯基磺酰胺的区域选择性环异构化提供了高产率的2-磺酰基甲基-1-苯并a庚因衍生物.这种7-Endo-Dig选择性环化反应通过不稳定的1-苯并氮杂中间体并入环外双键而进行的.环化底物...
    DOI:10.1039/c6Cc01061J

    海关参考信息

    专利信息


    专利号:WO-2024262824-A1
    优先权日:2023-06-20
    标 题 :Novel process for synthesis of polysubstituted pyridine derivatives
    发明人:PARK SEUNG BUM; YI SIHYEONG
    权利人:SEOUL NAT UNIV R&DB FOUNDATION
    摘要:The present invention relates to a novel method for synthesizing a polysubstituted pyridine derivative and, more specifically, to a method for synthesizing a 2,3,5-substituted pyridine derivative through a specific ring cleavage reaction. In the synthesis method of the present invention, an enamine structure is formed in situ by using beta keto ester/sulfone/phosphonic acid ester and ammonium acetate and subjected to an aldol condensation reaction with 3-formyl (aza) indole/benzofuran, a cyclization reaction, and a ring-cleavage reaction in that order to synthesize a characteristic pyridine structure having an alkyl/aryl substituent attached to the 2-position thereof, an ester/sulfone/phosphonic acid ester attached to the 3-position thereof, and ortho-aminoaryl/phenol including various substituents attached to the 5-position thereof. In particular, (aza)indole/benzofuran and beta keto ester/sulfone/phosphonic acid ester, which are reaction substrates, are substrates having very high accessibility, and enable the introduction of various substituents, thereby constructing a pyridine skeleton having high biocompatibility into which ortho-aminoaryl or phenol substituents having various substituents are introduced.

    专利号:US-4460786-A
    优先权日:1980-07-10
    标题 :Process for the selective addition of a compound having an activated carbon atom onto a substituted conjugated diene
    发明人:MOREL DIDIER
    权利人:RHONE POULENC IND
    摘要:The selective addition of a compound having an activated carbon atom onto the carbon atom in the 4-position of a buta-1,3-diene carrying a hydrocarbon substituent on the carbon atom in the 2-position is achieved by reacting the compound having the activated carbon atom with the buta-1,3-diene carrying the hydrocarbon substituent in water or in an aqueous-alcoholic mixture in the presence of a catalyst which consists of at least one water-soluble phosphine and at least one rhodium compound, the catalyst being in solution in the water or aqueous alcoholic mixture. The products obtained are useful as precursors of intermediates for the synthesis of vitamins and perfumes.

    专利号:US-4621165-A
    优先权日:1983-02-24
    标题 :Process for removing certain linear isoprene trimers from a mixture of isoprene trimers
    发明人:MOREL DIDIER
    权利人:RHONE POULENC SANTE
    摘要:A process for removing from a mixture of isoprene trimers compounds of the formula ##STR1## by reacting a mixture of cyclic and linear trimers with a compound having an activated carbon atom, of the formula: n n X--CH.sub.2 --Y n n in which one of X or Y is an electron-withdrawing group and the other is an electron-withdrawing or electron-donating group, in the presence of a catalyst consisting of a water-soluble phosphine and a rhodium compound, the reaction being carried out in water or in a water-alcohol medium, and separating the cyclic trimers and linear trimers containing the chain ##STR2## from the mixture of products of the formulae: ##STR3## which can be used, in particular, in the synthesis of vitamin E.

    专利号:US-4165330-A
    优先权日:1972-07-31
    标题 :Asymmetric synthesis via optically active chelating agents
    发明人:WHITNEY THOMAS A; LANGER JR ARTHUR W
    权利人:EXXON RESEARCH ENGINEERING CO
    摘要:An asymmetric synthesis process which involves addition of optically active chelated organometal compounds of lithium, sodium, beryllium, magnesium, zinc, copper and cadmium to prochiral unsaturated substrates. The optically active chelating agent is not consumed and can be recycled.

    专利号:CN-107188835-B
    优先权日:2017-06-14
    标题:A method of synthesis of a Fangya -type compound

    专利号:CN-109942560-B
    优先权日:2013-11-04
    标 题 :Macrocyclization reactions and intermediates useful in the synthesis of analogs of halichondrin B

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    合成参考文献


    摘要:Aitken, R. A.; Aitken, K. M., Science of Synthesis, (2010) 47, 1047.
    摘要:Grimmer, J.; Krieg, S.-C.; Manolikakes, G., Science of Synthesis Knowledge Updates, (2021) 1, 231.
    摘要:Rodriguez, J.; Bonne, D.; Coquerel, Y.; Constantieux, T., Science of Synthesis: Multicomponent Reactions, (2013) 2, 7.
    摘要:Llopis, Q.; Ayad, T.; Phansavath, P.; Ratovelomanana-Vidal, V., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2018) 2, 128.
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