化工学报 ›› 2019, Vol. 70 ›› Issue (S1): 110-114.DOI: 10.11949/j.issn.0438-1157.20181418
收稿日期:
2018-11-27
修回日期:
2018-12-11
出版日期:
2019-03-31
发布日期:
2019-03-31
通讯作者:
曾育才
作者简介:
曾育才(1961—),男,副教授,<email>mzzyc@jyu.edu.cn</email>
基金资助:
Yucai ZENG(),Xiaoling LIU,Qifeng LIANG,Jianquan LYU
Received:
2018-11-27
Revised:
2018-12-11
Online:
2019-03-31
Published:
2019-03-31
Contact:
Yucai ZENG
摘要:
微波辐射下,乙醇溶剂中K2CO3催化芳甲醛、丙二腈和α-萘酚(或β-萘酚)三组分一锅法快速合成了一系列2-氨基-3-氰基-4-芳基-4H-苯并[h]色烯或苯并[f]色烯衍生物。以苯甲醛、丙二氰与α-萘酚的反应为模板反应,通过单因素实验方案优化了反应的工艺条件。结果表明:反应物各10 mmol,催化剂K2CO3 1 mmol,溶剂无水乙醇15 ml,采用微波功率500 W,80℃回流反应 5 min,2-氨基-3-氰基-4-苯基-4H-苯并[h]色烯(4a)的收率83.6%。在上述最佳条件下,利用取代苯甲醛代替苯甲醛,4H-苯并[h]色烯衍生物(4)产率为65.8%~89.4%。 利用β-萘酚代替α-萘酚,4H-苯并[f]色烯衍生物(6)产率为67.5%~82.9%,合成产物通过熔点和红外光谱表征其结构。
中图分类号:
曾育才, 刘小玲, 梁奇峰, 吕鉴泉. 微波促进碳酸钾催化一锅法合成2-氨基-3氰基-4-芳基-4H-苯并色烯衍生物[J]. 化工学报, 2019, 70(S1): 110-114.
Yucai ZENG, Xiaoling LIU, Qifeng LIANG, Jianquan LYU. One-pot synthesis of 2-amino-4-aryl-3-cyano-4H-benzochromene derivatives catalyzed by K2CO3 under microwave irradiation[J]. CIESC Journal, 2019, 70(S1): 110-114.
序号 | 时间/min | 产率/% |
---|---|---|
1 | 3 | 65.5 |
2 | 5 | 83.6 |
3 | 8 | 79.4 |
4 | 10 | 76.0 |
5 | 12 | 71.5 |
表1 微波辐射时间对合成4a产率的影响
Table 1 Influence of microwave time on yield of synthetic 4a
序号 | 时间/min | 产率/% |
---|---|---|
1 | 3 | 65.5 |
2 | 5 | 83.6 |
3 | 8 | 79.4 |
4 | 10 | 76.0 |
5 | 12 | 71.5 |
序号 | 功率/W | 产率/% |
---|---|---|
1 | 200 | 46.8 |
2 | 300 | 65.6 |
3 | 400 | 77.4 |
4 | 500 | 83.6 |
5 | 600 | 78.5 |
表2 微波功率对合成4a产率的影响
Table 2 Influence of microwave power on yield of synthetic 4a
序号 | 功率/W | 产率/% |
---|---|---|
1 | 200 | 46.8 |
2 | 300 | 65.6 |
3 | 400 | 77.4 |
4 | 500 | 83.6 |
5 | 600 | 78.5 |
序号 | 温度/℃ | 产率/% |
---|---|---|
1 | 70 | 56.8 |
2 | 75 | 63.2 |
3 | 80 | 83.6 |
4 | 85 | 82.5 |
5 | 90 | 72.5 |
表3 微波辐射温度对合成4a产率的影响
Table 3 Influence of microwave temperature on yield of synthetic 4a
序号 | 温度/℃ | 产率/% |
---|---|---|
1 | 70 | 56.8 |
2 | 75 | 63.2 |
3 | 80 | 83.6 |
4 | 85 | 82.5 |
5 | 90 | 72.5 |
序号 | 碳酸钾用量/mmol | 产率/% |
---|---|---|
1 | 0.0 | 0 |
2 | 0.5 | 65.0 |
3 | 1.0 | 83.6 |
4 | 1.5 | 81.5 |
5 | 2.0 | 79.0 |
表4 碳酸钾用量对合成4a产率的影响
Table 4 Influence of catalyst dosage on yield of synthetic 4a
序号 | 碳酸钾用量/mmol | 产率/% |
---|---|---|
1 | 0.0 | 0 |
2 | 0.5 | 65.0 |
3 | 1.0 | 83.6 |
4 | 1.5 | 81.5 |
5 | 2.0 | 79.0 |
溶剂 | 用量/ml | 产率/% |
---|---|---|
蒸馏水 | 15 | 0 |
95%乙醇 | 15 | 45.0 |
无水乙醇 | 10 | 80.5 |
无水乙醇 | 15 | 83.6 |
无水乙醇 | 20 | 79.6 |
无溶剂 | 0 | 0 |
表5 溶剂及其用量对合成4a产率的影响
Table 5 Influence of solvent and its dosage on yield of synthetic 4a
溶剂 | 用量/ml | 产率/% |
---|---|---|
蒸馏水 | 15 | 0 |
95%乙醇 | 15 | 45.0 |
无水乙醇 | 10 | 80.5 |
无水乙醇 | 15 | 83.6 |
无水乙醇 | 20 | 79.6 |
无溶剂 | 0 | 0 |
产物 | Ar | 产率/% | 熔点(文献)/℃ | 产物IR数据(KBr压片)ν/cm-1 |
---|---|---|---|---|
4a | C6H5 | 83.6 | 207—208(210—211)[ | 3447, 3305, 3182, 2203, 1655 1632, 1605, 1573, 1400, 1374, 1261, 1185, 806, 742, 698 |
4b | 2,4-Cl2C6H3 | 89.4 | 217—219(216—217)[ | 3448, 3334, 3120, 2192, 1665, 1599, 1572, 1411, 1375, 1261, 1189, 1106, 830, 809, 735 |
4c | 4-ClC6H4 | 81.5 | 234—235(232—234)[ | 3454, 3330, 2194, 1669, 1602, 1572, 1489, 1407, 1376, 1261, 1189, 1103, 802, 764 |
4d | 4-MeOC6H4 | 69.5 | 198—200(196—198)[ | 3413, 3324, 3204, 2193, 1662, 1603, 1574, 1509, 1408, 1376, 1252, 1192, 1104, 801, 762 |
4e | 4-Me2NC6H4 | 65.8 | 201—203(200—202)[ | 3416, 3328, 3059, 2194, 1661, 1607, 1576, 1508, 1405, 1375, 1250, 1190, 1103, 802, 760 |
6a | C6H5 | 78.9 | 275—277(278—280)[ | 3429, 3336, 3048, 2184, 1646, 1588, 1513,1401, 1279, 1255, 1182, 798, 749, 700 |
6b | 2,4-Cl2C6H3 | 82.9 | 230—232(228—230)[ | 3458, 3326, 3066, 2197, 1662, 1604, 1513, 1486, 1406, 1282, 1256, 1186, 836, 813, 758 |
6c | 4-ClC6H4 | 78.8 | 223—224(224—226)[ | 3460, 3324, 3069, 2194, 1650, 1590, 1514, 1489, 1408, 1280, 1259, 1187, 816, 775, 746 |
6d | 4-MeOC6H4 | 67.5 | 180—182(182—183)[ | 3419, 3323, 3060, 2190, 1660, 1601, 1573, 1506, 1406, 1279, 1257, 1180, 810, 769, 746 |
6e | 4-MeC6H4 | 70.6 | 269—272(270—272)[ | 3431, 3339, 3058, 2187, 1642, 1590, 1510, 1407, 1235, 1214, 1181, 819, 790, 765 |
表6 不同反应底物对合成产率的影响
Table 6 Influence of different reaction substrates on yield of target products
产物 | Ar | 产率/% | 熔点(文献)/℃ | 产物IR数据(KBr压片)ν/cm-1 |
---|---|---|---|---|
4a | C6H5 | 83.6 | 207—208(210—211)[ | 3447, 3305, 3182, 2203, 1655 1632, 1605, 1573, 1400, 1374, 1261, 1185, 806, 742, 698 |
4b | 2,4-Cl2C6H3 | 89.4 | 217—219(216—217)[ | 3448, 3334, 3120, 2192, 1665, 1599, 1572, 1411, 1375, 1261, 1189, 1106, 830, 809, 735 |
4c | 4-ClC6H4 | 81.5 | 234—235(232—234)[ | 3454, 3330, 2194, 1669, 1602, 1572, 1489, 1407, 1376, 1261, 1189, 1103, 802, 764 |
4d | 4-MeOC6H4 | 69.5 | 198—200(196—198)[ | 3413, 3324, 3204, 2193, 1662, 1603, 1574, 1509, 1408, 1376, 1252, 1192, 1104, 801, 762 |
4e | 4-Me2NC6H4 | 65.8 | 201—203(200—202)[ | 3416, 3328, 3059, 2194, 1661, 1607, 1576, 1508, 1405, 1375, 1250, 1190, 1103, 802, 760 |
6a | C6H5 | 78.9 | 275—277(278—280)[ | 3429, 3336, 3048, 2184, 1646, 1588, 1513,1401, 1279, 1255, 1182, 798, 749, 700 |
6b | 2,4-Cl2C6H3 | 82.9 | 230—232(228—230)[ | 3458, 3326, 3066, 2197, 1662, 1604, 1513, 1486, 1406, 1282, 1256, 1186, 836, 813, 758 |
6c | 4-ClC6H4 | 78.8 | 223—224(224—226)[ | 3460, 3324, 3069, 2194, 1650, 1590, 1514, 1489, 1408, 1280, 1259, 1187, 816, 775, 746 |
6d | 4-MeOC6H4 | 67.5 | 180—182(182—183)[ | 3419, 3323, 3060, 2190, 1660, 1601, 1573, 1506, 1406, 1279, 1257, 1180, 810, 769, 746 |
6e | 4-MeC6H4 | 70.6 | 269—272(270—272)[ | 3431, 3339, 3058, 2187, 1642, 1590, 1510, 1407, 1235, 1214, 1181, 819, 790, 765 |
1 | 黄邦洲, 朱天民, 于学君, 等. 2H-苯并吡喃类化合物的 简便合成方法[J]. 有机化学, 1989, 9(6): 552-554. |
HuangB Z, ZhuT M, YuX J, et al. A convenient route for the synthesis of 2H-1-benzopyranes[J]. Chinese Journal of Organic Chemistry, 1989, 9(6): 552-554. | |
2 | GoutamB, BubunB.Facile and one-pot access to diverse and densely functionalized -amino-3-cyano-4H-pyrans and pyran-annulated heterocyclic scaffolds via an ecofriendly multicomponent reaction at room temperature using urea as a novel organo-catalyst[J]. ACS Sustainable Chem. Eng., 2014, 2: 411-422. |
3 | LiW J, LiuH, JiangX F, et al. Enantioselective organocatalytic conjugate addition of nitroalkanes to electrophilic 2-iminochromenes[J]. ACS Catal., 2012, 2: 1535-1538. |
4 | KemnI W, KasibhatlaS, JiangS. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell and caspase-based high-throughput screening assay(2): Structure- activity relationships of the 7-and 5-, 6-, 8-positions[J]. Bioorganic & Medicinal Chemistry Letters, 2005, 15: 4745-4751. |
5 | KemnI W, DreweJ, JiangS. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell and caspase-based high-throughput screening assay structure-activity relationships of the 4-aryl group[J]. J. Med. Chem., 2004, 47: 6299-6310. |
6 | ZhangG, ZhangY H, YanJ X, et al. One-pot enantioselective synthesis of functionalized pyranocoumarins and 2-amino-4H-chromenes: discovery of a type of potent antibacterial agent[J]. J. Org. Chem., 2012, 77: 878-888. |
7 | 王喜存, 许新兵, 权正军, 等. PEG-400 为绿色反应介质无催化一锅法合成 2-氨基-3-氰基-4-芳基-4H-苯并色烯衍生物[J].有机化学, 2009, 29(11): 1821-1824. |
WangX C, XuX B, QuanZ J, et al. Synthesis of 2-amino-3-cyano-4-arylbenzochromenes under noncatalysis conditions using PEG-400 as green medium[J]. Chinese Journal of Organic Chemistry, 2009, 29(11): 1821-1824. | |
8 | 周杰兴, 王香善, 曾兆森, 等. KF-Al2O3催化下二-γ-吡喃并[2,3-a;2',3'-f]萘衍生物的合成[J]. 有机化学, 2007, 27(6): 786-789. |
ZhouJ X, WangX S, ZengZ S, et al. Synthesis of di-γ-pyrano[2,3-a;2',3'-f]naphthalene derivatives catalyzed by KF/Al2O3[J]. Chinese Journal of Organic Chemistry, 2007, 27(6): 786-789. | |
9 | 章明, 张爱琴, 黄仁生, 等. 无溶剂CTAB催化制备取代2-氨基-2-色烯[J]. 化学试剂, 2006, 28(8): 491-492. |
ZhangM, ZhangA Q, HuangR S, et al. CTAB catalyzed preparation of substituted 2-amino-2-chromene under solvent free condition[J]. Chemical Reagents, 2006, 28(8): 491-492. | |
10 | 史达清, 王香善, 屠树江. KF/ Al2O3催化下4H-色烯衍生物的合成[J]. 有机化学, 2002, 22(12): 1053-1056. |
ShiD Q, WangX S, TuS J. Synthesis of 4H-chromene derivatives catalyzed by KF/Al2O3[J]. Chinese Journal of Organic Chemistry, 2002, 22(12): 1053-1056. | |
11 | SaeedB, SorourR, MortezaB, et al. DABCO-catalyzed efficient synthesis of naphthopyran derivatives via one-pot three component condensation reaction at room temperature [J]. Synthetic Commun, 2008, 38: 1078-1089. |
12 | 孙宏伟, 王浩宇, 连春霞, 等. DABCO催化的“一锅法”水相合成苯并色烯衍生物[J]. 合成化学, 2011, 19(3): 370-372. |
SunH W, WangH Y, LianC X, et al. DABCO-catalyzed synthesis of benzo[g]chromene derivatives in water by one-pot method[J]. Chinese Journal of Synthetic Chemistry, 2011, 19(3): 370-372. | |
13 | 陈路, 李毅群, 黄旭江, 等. 乙二胺四乙酸四钠“一锅法”催化合成2-氨基-2-色烯衍生物[J]. 有机化学, 2009, 29(3): 437-440. |
ChenL, LiY Q, HuangX J, et al. One-pot synthesis of 2-amino-2-chromenes catalyzed by tetrasodium ethylenediaminetetraacetate[J]. Chinese Journal of Organic Chemistry, 2009, 29(3): 437-440. | |
14 | KhuranaJ M, NandB, SalujaP. DBU: a highly efficient catalyst for one-pot synthesis of substituted 3,4-dihydropyrano[3,2-c]chromenes, dihydropyrano[4,3-b]pyranes, 2-amino-4H-benzo[h]chromenes and 2-a-mino-4H-benzo[g]chromenes in aqueous medium[J]. Tetrahedron, 2010, 66: 5637-5641. |
15 | SeyedM B, NiloufarIR, HamedT. Nanozeoliteclino ptilolite as a highly efficient heterogeneous catalyst for the synthesis of various 2-amino-4H-chromene derivatives inaqueous media[J]. Green Chem., 2013, 15: 3446-3458. |
16 | DekaminM G, EslamiM. Highly efficient organo catalytic synthesis of diverse and densely functionalized 2-amino-3-cyano-4H-pyrans under mechanochemical ball milling[J]. Green Chem., 2014, 16: 4914-4921. |
17 | NourallahH, MalekT M, MirR M, et al. Potassium sodium tartrate as a versatile and efficient catalyst for the one-pot synthesis of pyran annulated heterocyclic compounds in aqueous media[J]. Res. Chem. Intermed., 2015, 41: 169-174. |
18 | 窦辉, 高思旖, 付召龙, 等. 新型氨基功能化碱性离子液体1-(2-氨基乙基)-3-甲基咪唑咪唑盐催化四类取代2-氨基-4H-色烯衍生物的合成[J]. 有机化学, 2011, 31(7): 1056-1063. |
DouH, GaoS Y, FuZ L, et al. Improved synthesis of substituted 2-amino-4H-chromene derivatives catalyzed by a new amino-functionalized basic ionic liquid 1-(2-aminoethyl)-3-methylimidazolium imidazolide[J]. Chinese Journal of Synthetic Chemistry, 2011, 31(7): 1056-1063. | |
19 | 王英磊, 陈靖, 王玉东, 等. 低毒、易降解离子液体三乙醇胺乙酸盐催化合成2-氨基-4H-苯并色烯衍生物[J]. 南阳理工学院学报, 2017, 9(2): 99-103. |
WangY L, ChenJ, WangY D, et al. Synthesis of 2-amino-4H-benzochromene derivatives by low toxic and readily-biodegradable ionic liquid triethanolammonium acetate[J]. Journal of Nanyang institute of Technology, 2017, 9(2): 99-103. | |
20 | MithuS, BabulalD, AmartaK P. Synthesis of pyran derivatives under ultrasound irradiation using Ni nanoparticles as reusable catalysts in aqueous medium[J]. Comptes Rendus Chimie, 2013, 16: 1079-1085. |
21 | 李佰林, 李红艳, 程优. 酸性离子液体催化2-氨基-2-色烯的高能球磨法合成[J]. 化学试剂, 2014, 36(11): 1045-1049. |
LiB L, LiH Y, ChengY. Efficient synthesis of 2-amino-2-chromenes by high energy ball milling catalysized by acidic ionic | |
liquids[J]. Chemical Reagents, 2014, 36(11): 1045-1049. | |
22 | 栾长军, 王建强, 张国华, 等. 无催化剂条件下微波辐射一步法合成2-氨基-4-芳基-5-氧代-5,6,7,8-四氢-4H-苯并吡喃-3-腈 [J]. 有机化学, 2011, 31(6): 860-864. |
LuanC J, WangJ Q, ZhangG H, et al. One-pot synthesis of 2-amino-4-aryl-5-oxo-5,6,7,8-tetrahydro-4H-benzopyran-3- carbonitrile under microwave irradiation without catalyst[J]. Chinese Journal of Organic Chemistry, 2011, 31(6): 860-864. | |
23 | 曾育才, 刘小玲, 温运明, 等. K2CO3催化合成2-氨基-4H-色烯衍生物[J]. 精细化工, 2014, 31(12): 1522-1525. |
ZengY C, LiuX L, WenY M, et al. Synthesis of 2-amino-4H-chromene derivatives catalyzed by K2CO3[J]. Fine Chemicals, 2014, 31(12): 1522-1525. |
[1] | 毛桃嫣, 邹敏婷, 郑成, 曾昭文, 伍旭贤, 肖润辉, 彭思玉. 微波化学反应的无量纲准数动力学模型研究:以偶氮二异丁脒盐酸盐(AIBA)分解反应为例[J]. 化工学报, 2021, 72(3): 1364-1371. |
[2] | 秦宁, 闵清, 邵开元, 胡文祥. 间甲基苯甲脒盐酸盐的合成研究[J]. 化工学报, 2019, 70(S1): 242-247. |
[3] | 李颖, 刘肖红, 安华良, 赵新强, 王延吉. Ni/La-Al2O3的制备及催化正丁醛“一锅法”合成辛醇反应性能[J]. 化工学报, 2017, 68(4): 1381-1389. |
[4] | 田禾青, 王维龙, 丁静, 郭祥. 微波法制备膨胀石墨及其膨胀特性[J]. 化工学报, 2015, 66(S1): 354-358. |
[5] | 韩洪军, 牟晋铭, 马文成, 贾胜勇. 微波辐射对青霉素菌渣破壁效果的影响[J]. 化工学报, 2013, 64(10): 3812-3817. |
[6] | 宁慧青1,卢兴鲁2,刘 泉2,任 军2,李 忠2. 固态离子交换制备Cu(Ⅰ)分子筛研究进展[J]. 化工进展, 2012, 31(09): 1950-1958. |
[7] | 王宏晓1,2,商士斌1,2,徐 徐1,2,谭卫红1,2. 微波辐射条件下丙烯海松酸的合成 [J]. CIESC Journal, 2011, 30(7): 1602-. |
[8] | 成西涛1,2,李稳宏1,唐 璇3,张存社2,吴素芳2,白 燕2. 微波辐射下聚醚改性聚硅氧烷的合成及其乳液的性能[J]. CIESC Journal, 2011, 30(12): 2732-. |
[9] | 孙宏伟1,陈建峰2. 我国化工过程强化技术理论与应用研究进展 [J]. CIESC Journal, 2011, 30(1): 1-. |
[10] | 徐 琼1,邹丽霞1,2,熊小青1. 纳米WO3·NiO·0.33H2O光催化剂的结构与性能 [J]. CIESC Journal, 2010, 29(2): 260-. |
[11] | 谯志勇,李明春,辛梅华,高 伟. 微波辐射在壳聚糖化学改性中的应用研究进展 [J]. CIESC Journal, 2009, 28(3): 412-. |
[12] | 舒 静,任丽丽,张铁珍,王 鉴,王 刚. 微波辐射在催化剂制备中的应用 [J]. CIESC Journal, 2008, 27(3): 352-. |
[13] | 肖祖峰,陈明东,韩光泽. 电磁场作用下的强化传质研究进展 [J]. CIESC Journal, 2008, 27(12): 1911-. |
[14] | 罗志刚; 于淑娟 ;杨连生. 微波场对小麦淀粉性质的影响 [J]. CIESC Journal, 2007, 58(11): 2871-2875. |
[15] | M.Kamel,J.I.Lombrana,C.deElvira,R.Rodríguez. 微波及辐射真空干燥过程中的干燥动力学及能量消耗[J]. CIESC Journal, 2004, 12(6): 809-813. |
阅读次数 | ||||||
全文 |
|
|||||
摘要 |
|
|||||