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对叔丁基杯[n](n=6,8)芳烃O-烃基化衍生物的微波辐射合成 被引量:1
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作者 安琳 王晨 +2 位作者 张玲 薛运生 牟杰 《化学试剂》 CAS CSCD 北大核心 2011年第11期1051-1053,共3页
在微波辐射条件下,以对叔丁基杯[6]、杯[8]芳烃为原料,采用氯化苄、碘代正丁烷、溴代正戊烷为烃基化试剂,PEG-400为催化剂,制备了标题化合物,通过IR、1HNMR光谱对产物的结构进行表征。微波辐射约5 min,即可得到收率中等(40%~66%)的对... 在微波辐射条件下,以对叔丁基杯[6]、杯[8]芳烃为原料,采用氯化苄、碘代正丁烷、溴代正戊烷为烃基化试剂,PEG-400为催化剂,制备了标题化合物,通过IR、1HNMR光谱对产物的结构进行表征。微波辐射约5 min,即可得到收率中等(40%~66%)的对叔丁基杯芳烃O-烃基化衍生物。结果表明微波辐射法操作简单、反应时间大大缩短、污染明显减少。 展开更多
关键词 微波辐射 杯芳烃 o-烃基化
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TBHPAS催化苯酚的O-烃基化及酰胺和酰亚胺在KF/Al_2O_3协同下的N-烃基化反应 被引量:1
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作者 张传新 司晚龄 +1 位作者 郭保国 刘振中 《商丘师范学院学报》 CAS 2001年第4期73-76,共4页
TBHPAS固 液相转移催化苯酚的O 烃基化及在KF/Al2 O3 协同作用下固 液相转移催化酰胺和酰亚胺的N 烃基化反应 ,取得了理想的收率 ,方法简单 ,操作方便 ,反应条件温和 ,是一种较为理想的O和N 烃基化方法 .
关键词 TBHPAS 固-液相转移催 酰胺 酰亚胺 o-烃基化 N-烃基 KF/Al2O3协同 苯酚 有机合成
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Cu_2O/SiC as efficient catalyst for Ullmann coupling of phenols with aryl halides 被引量:1
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作者 Yibing Wang Xiaoning Guo +3 位作者 Manqian Lü Zhaoyang Zhai Yingyong Wang Xiangyun Guo 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2017年第4期658-664,共7页
A Cu2O/SiC heterogeneous catalyst was prepared via a two‐step liquid‐phase method using diethyleneglycol as both the solvent and the reducing agent.The catalyst was characterized using X‐raydiffraction,X‐ray photo... A Cu2O/SiC heterogeneous catalyst was prepared via a two‐step liquid‐phase method using diethyleneglycol as both the solvent and the reducing agent.The catalyst was characterized using X‐raydiffraction,X‐ray photoelectron spectroscopy,scanning electron microscopy(SEM),transmissionelectron microscopy(TEM),and H2temperature‐programmed reduction.All the results indicatethat Cu is present on the SiC support primarily as Cu2O.The SEM and TEM results show that cubicCu2O nanoparticles are uniformly dispersed on theβ‐SiC surface.The reaction conditions,namelythe temperature,reaction time,and amounts of base and catalyst used,for the Ullmann‐type C–Ocross‐coupling reaction were optimized.A model reaction was performed using iodobenzene(14.0mmol)and phenol(14.0mmol)with Cu2O/SiC(5wt%Cu)as the catalyst,Cs2CO3(1.0equiv.)as thebase,and tetrahydrofuran as the solvent at150°C for3h;a yield of97%was obtained and theturnover frequency(TOF)was1136h?1.The Cu2O/SiC catalyst has a broad substrate scope and canbe used in Ullmann‐type C–O cross‐coupling reactions of aryl halides and phenols bearing a varietyof different substituents.The catalyst also showed high activity in the Ullmann‐type C–Scross‐coupling of thiophenol with iodobenzene and substituted iodobenzenes;a TOF of1186h?1was achieved.The recyclability of the Cu2O/SiC catalyst in the O‐arylation of phenol with iodobenzenewas investigated under the optimum conditions.The yield decreased from97%to64%afterfive cycles.The main reason for the decrease in the catalyst activity is loss of the active component,i.e.,Cu2O. 展开更多
关键词 Cuprous oxide Silica carbide Ullmann coupling O‐arylation PHENOLS Aryl halide
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