2</sub> 保護下 <img src="/qkimages/hnzy/hnzy202504/hnzy20250411-1-l.jpg" with="47px" style="vertical-align: middle;"> 反應(yīng) 12h 在底物范圍擴展中有效得到一系列二氫查爾酮化合物,經(jīng) <sup>1</sup>H NMR、 <sup>13</sup>C NMR以及HR-ESI-MS確證其結(jié)構(gòu)。結(jié)論單質(zhì)硫/水/1,4-二氮雜二環(huán)[2.2.2]辛烷/N,N-二甲基甲酰胺體系可以選擇性還原查爾酮制備二氫查爾酮,該方法具有底物適用范圍廣,綠色環(huán)保、操作簡單、產(chǎn)率優(yōu)良的特點。-龍源期刊網(wǎng)" />

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單質(zhì)硫催化查爾酮類化合物選擇性還原制備二氫查爾酮的研究

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[中圖分類號]R284.3 [文獻標志碼]A [文章編號]doi:10.3969/j.issn.1674-070X.2025.04.011

[Abstract]Objective To investigate thesynthetic method for preparing dihydrochalcones byselectivelyreducing chalcones using water asthehydrogensourceunderthecatalysisof elemental sulfur.Methods Chalcone wasusedasa model substrateto investigatetheoptialreactionconditions,andthinfluenceofdfrenttypesofsubstituentsonthereactionyieldwasexamined. Results Theoptialreactionconditionwereasfolows:0.5mmolofchalcone,1.25equivalentsofelementalsulfur,2.5quivalents of 1,4-diazabicyclo [2.2.2]octane, 400μL of water,and 2.5 mL of N,N-dimethylformamide,with the reaction conducted at 120°C for 12hunderN2protectionAseriesofdihydrochalcones wereefectivelyobtainedintheexpansionofthesubstratescope,andtheir structures were confirmed by 1H -NMR, 13C -NMR, and HR-ESI-MS. Conclusion The system of elemental sulfur/water/l, 4- (204號 diazabicyclo2ctane/N,dimetyforaideanselecivelyducechaonetodrohalcone.Thsmethdfaturawide range of applicable substrates, environmental friendliness, simple operation, and excellent yield.

[Keywords] elemental sulfur; chalcone;dihydrochalcone; selective reduction; synthesis

二氫查爾酮類化合物屬于查爾酮家族的主要成員,含有1,3-二苯基丙酮基本骨架。(剩余11295字)

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