商丘师范学院学报
商丘師範學院學報
상구사범학원학보
JOURNAL OF SHANGQIU TEACHERS COLLEGE
2014年
12期
53-57
,共5页
H3 PW12 O40/TiO2 -SiO2%3,4-二氢嘧啶酮
H3 PW12 O40/TiO2 -SiO2%3,4-二氫嘧啶酮
H3 PW12 O40/TiO2 -SiO2%3,4-이경밀정동
H3 PW12 O40/TiO2 -SiO2%3,4 -dihydropyrimidinone
以H3 PW12 O40/TiO2-SiO2为催化剂,取代苯甲醛、乙酰乙酸乙酯和尿素为原料,无水乙醇为溶剂合成3,4-二氢嘧啶-2(1H)-酮衍生物.探讨了原料物质的量比、反应温度、催化剂用量及反应时间对收率的影响.实验表明:固定取代苯甲醛的用量为0.04 mol和无水乙醇的量为15 mL的情况下,n(取代苯甲醛)∶n(乙酰乙酸乙酯)∶n(尿素)=1∶1.0∶1.5,催化剂的用量占反应物料总质量的1.5%,反应温度为90℃,反应时间为75 min,分别以对羟基苯甲醛、对硝基苯甲醛、茴香醛、4-氯苯甲醛、对甲氧基苯甲醛分别代替苯甲醛,产品收率为35.0%-89.2%.催化剂和合成产品分别采用IR, XRD和1 H NMR, IR, MS手段进行表征.
以H3 PW12 O40/TiO2-SiO2為催化劑,取代苯甲醛、乙酰乙痠乙酯和尿素為原料,無水乙醇為溶劑閤成3,4-二氫嘧啶-2(1H)-酮衍生物.探討瞭原料物質的量比、反應溫度、催化劑用量及反應時間對收率的影響.實驗錶明:固定取代苯甲醛的用量為0.04 mol和無水乙醇的量為15 mL的情況下,n(取代苯甲醛)∶n(乙酰乙痠乙酯)∶n(尿素)=1∶1.0∶1.5,催化劑的用量佔反應物料總質量的1.5%,反應溫度為90℃,反應時間為75 min,分彆以對羥基苯甲醛、對硝基苯甲醛、茴香醛、4-氯苯甲醛、對甲氧基苯甲醛分彆代替苯甲醛,產品收率為35.0%-89.2%.催化劑和閤成產品分彆採用IR, XRD和1 H NMR, IR, MS手段進行錶徵.
이H3 PW12 O40/TiO2-SiO2위최화제,취대분갑철、을선을산을지화뇨소위원료,무수을순위용제합성3,4-이경밀정-2(1H)-동연생물.탐토료원료물질적량비、반응온도、최화제용량급반응시간대수솔적영향.실험표명:고정취대분갑철적용량위0.04 mol화무수을순적량위15 mL적정황하,n(취대분갑철)∶n(을선을산을지)∶n(뇨소)=1∶1.0∶1.5,최화제적용량점반응물료총질량적1.5%,반응온도위90℃,반응시간위75 min,분별이대간기분갑철、대초기분갑철、회향철、4-록분갑철、대갑양기분갑철분별대체분갑철,산품수솔위35.0%-89.2%.최화제화합성산품분별채용IR, XRD화1 H NMR, IR, MS수단진행표정.
3, 4 -Dihydropy -rimidine -2 ( 1H ) -one was synthesized from substituted benzaldehyde, ethylacetoacetate and urea using H3 PW12 O40/TiO2 -SiO2 as a novel eco-friendly catalyst that prepared by a sol-gel technique.The influences of molar ratio of reactant, reaction temperature, catalyst dosage and reaction time were discussed.Experimental results showed that H3 PW12 O40/TiO2 -SiO2 is a good catalyst for synthesis of 3,4-dihydropy-rimidine-2(1H) -one.When the dosage of substituted benzaldehyde is 0.04 mol, and anhydrous ethanol as solvent,n(substituted benzaldehyde)∶n(ethyl acetoacetate)∶n(urea) =1.0∶1.0∶1.5, the quantity of catalyst is 1.5%quantity of the feed stock, and reaction temperature is 90℃, and reaction time 75 min, the yield of 3,4-dihydropyrimidine-2(1H)-one could reach 35.0%-89.2%.The catalyst and synthesis products were characterized by IR, XRD and 1H NMR, IR, MS, respectively.