CN102241638A - 一种吩嗪-2,3二胺盐酸盐的合成方法 - Google Patents

一种吩嗪-2,3二胺盐酸盐的合成方法 Download PDF

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CN102241638A
CN102241638A CN2011101026698A CN201110102669A CN102241638A CN 102241638 A CN102241638 A CN 102241638A CN 2011101026698 A CN2011101026698 A CN 2011101026698A CN 201110102669 A CN201110102669 A CN 201110102669A CN 102241638 A CN102241638 A CN 102241638A
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synthesis method
diamine hydrochloride
phenazine
diamine
azophenlyene
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罗梅
冯海涛
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Abstract

一种吩嗪-2,3二胺盐酸盐的合成方法,包括合成和分离,其特征在于吩嗪-2,3二胺盐酸盐合成方法,以邻苯二胺与二水合氯化铜为原料,包括合成、分离、结晶和洗涤,其特征在于2.06∶1的邻苯二胺与氯化铜在乙腈溶剂中加热回流24h,反应后热过滤,对滤渣用DMF和无水乙醚配成饱和溶液后密封,一天后底部有棕色晶体出现。

Description

一种吩嗪-2,3二胺盐酸盐的合成方法
一、技术领域
本发明涉及一种有机精细化学品的合成方法,确切地说是一种吩嗪-2,3二胺盐酸盐的合成方法。
二、背景技术
吩嗪-2,3二胺的合成方法已有许多文献报道。在1989年,Journal of Heterocyclic Chemistry,报道了该化合物的合成方法,随后,许多文献又相继报道了该物质的合成方法。
1.Crank,G.;Makin,M.I.H.Journal of Heterocyclic Chemistry,1989,26(4),1163-5.
2.Chauhan,Shive Murat Singh;Bisht,Tanuja;Garg,Bhaskar.Tetrahedron Letters 2008,49(47),6646-6649.
3.Kaizer,Jozsef;Csonka,Robert;Speier,Gabor.Reaction Kinetics and Catalysis Letters2002,75(2),367-374.
申请人在合成邻苯二胺氯化铜配合物的实验中,意外地得到了另一种化合物吩嗪-2,3二胺盐酸盐。
三、发明内容
本发明旨在提供化合物吩嗪-2,3二胺盐酸盐,所要解决的技术问题是一步合成得到目标产物。
本合成方法包括合成和分离,所述的合成2∶1的邻苯二胺与氯化铜在中反应24小时后,反应后热过滤,对滤渣用DMF和无水乙醚配成饱和溶液后密封,一天后底部有棕色晶体出现。
合成反应如下:
Figure BSA00000480109500011
本合成方法一步得到目标产物,工艺简单,操作方便。
其反应机理可推测如下:
两分子邻苯二胺,在氯化铜的作用下,首先分子间脱去2分子氢气,形成吩嗪-2,3二胺,然后与溶液中产生的盐酸生成吩嗪-2,3二胺盐酸盐。
本合成方法一步得到目标产物,工艺简单,操作方便。
四、附图说明
图1是吩嗪-2,3二胺盐酸盐的X-衍射分析图。
五、具体实施方式
100mL两口瓶中,无水无氧条件下,加入30mL乙腈,邻苯二胺1.1216g(10.3mmol),二水合氯化铜0.8526g(4.98mmol),加热回流24h,反应后热过滤,对滤渣用DMF和无水乙醚配成饱和溶液后密封,一天后底部有棕色晶体出现。元素分析:C:56.5800H:5.0062N:21.2063,IR(KBr压片):3286,3194,3119,1679,1624,1526,1371,1237,1149,756,726,612,586.

Claims (1)

1.一种吩嗪-2,3二胺盐酸盐的合成方法,包括合成和分离,其特征在于吩嗪-2,3二胺盐酸盐合成方法,以邻苯二胺与二水合氯化铜为原料,包括合成、分离、结晶和洗涤,其特征在于2.06∶1的邻苯二胺与氯化铜在乙腈溶剂中加热回流24h,反应后热过滤,对滤渣用DMF和无水乙醚配成饱和溶液后密封,一天后底部有棕色晶体出现。
CN2011101026698A 2011-04-22 2011-04-22 一种吩嗪-2,3二胺盐酸盐的合成方法 Pending CN102241638A (zh)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4550174A (en) * 1983-06-25 1985-10-29 Hoechst Aktiengesellschaft Process for reducing the proportions of by products in the preparation of carbendazim
CN101914070A (zh) * 2010-08-16 2010-12-15 罗梅 一种吩嗪-2,3-二胺盐酸盐的合成方法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4550174A (en) * 1983-06-25 1985-10-29 Hoechst Aktiengesellschaft Process for reducing the proportions of by products in the preparation of carbendazim
CN101914070A (zh) * 2010-08-16 2010-12-15 罗梅 一种吩嗪-2,3-二胺盐酸盐的合成方法

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
SANDOR NEMETH,ET.AL: "cobalt(II) ion catalyzed oxidative cyclization of o-phenylenedlamine in the presence of dioxygen.synthesis of substituted 2H-benzimidazoles and 2,3-diaminophenazine", 《JOURNAL OF MOLECULAR CATALYSIS》 *
SHIE-MING PENG: "Cu(II) ion catalytic oxidation of o-phenylenediamine and diaminomaleonitrile and the crystal structure of the final products (C12N4H11)(ClO4)-H2O and [Cu5(CN)6(dmf)4]", 《INORGANICA CHIMICA ACTA》 *
姜远良,冯春梁: ""辣根过氧化物酶催化合成2,3-二氨基吩嗪及其光谱表征"", 《光谱实验室》 *

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Application publication date: 20111116