CN103664761A - 一种4-吡啶酚的制备方法 - Google Patents
一种4-吡啶酚的制备方法 Download PDFInfo
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- CN103664761A CN103664761A CN201310646586.4A CN201310646586A CN103664761A CN 103664761 A CN103664761 A CN 103664761A CN 201310646586 A CN201310646586 A CN 201310646586A CN 103664761 A CN103664761 A CN 103664761A
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- pyridol
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- pyridyl
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- GCNTZFIIOFTKIY-UHFFFAOYSA-N 4-hydroxypyridine Chemical compound OC1=CC=NC=C1 GCNTZFIIOFTKIY-UHFFFAOYSA-N 0.000 title claims abstract description 26
- 238000002360 preparation method Methods 0.000 title claims abstract description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims abstract description 18
- UZUCHEKZABBQDF-UHFFFAOYSA-N 4-(2H-pyridin-1-yl)pyridine hydrochloride Chemical compound [Cl-].N1(CC=CC=C1)C1=CC=[NH+]C=C1 UZUCHEKZABBQDF-UHFFFAOYSA-N 0.000 claims abstract description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000006243 chemical reaction Methods 0.000 claims abstract description 12
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims abstract description 12
- 230000035484 reaction time Effects 0.000 claims abstract description 8
- 239000000376 reactant Substances 0.000 claims abstract description 7
- 238000001914 filtration Methods 0.000 claims abstract description 6
- 238000010438 heat treatment Methods 0.000 claims abstract description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000126 substance Substances 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 230000002378 acidificating effect Effects 0.000 claims abstract description 5
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical group [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- 238000001556 precipitation Methods 0.000 claims description 5
- OENLEHTYJXMVBG-UHFFFAOYSA-N pyridine;hydrate Chemical compound [OH-].C1=CC=[NH+]C=C1 OENLEHTYJXMVBG-UHFFFAOYSA-N 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 230000001105 regulatory effect Effects 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 10
- 238000004519 manufacturing process Methods 0.000 abstract description 4
- 239000006227 byproduct Substances 0.000 abstract description 3
- 238000003786 synthesis reaction Methods 0.000 abstract description 3
- 238000002156 mixing Methods 0.000 abstract 2
- 239000002244 precipitate Substances 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000001376 precipitating effect Effects 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 206010007559 Cardiac failure congestive Diseases 0.000 description 1
- 206010019280 Heart failures Diseases 0.000 description 1
- NGBFQHCMQULJNZ-UHFFFAOYSA-N Torsemide Chemical compound CC(C)NC(=O)NS(=O)(=O)C1=CN=CC=C1NC1=CC=CC(C)=C1 NGBFQHCMQULJNZ-UHFFFAOYSA-N 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000002934 diuretic Substances 0.000 description 1
- 230000001882 diuretic effect Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 231100000652 hormesis Toxicity 0.000 description 1
- 235000019633 pungent taste Nutrition 0.000 description 1
- 210000002345 respiratory system Anatomy 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229960005461 torasemide Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/68—One oxygen atom attached in position 4
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
本发明公开了一种4-吡啶酚的制备方法,包括步骤为:将吡啶和乙酸乙酯混合放入到微波炉中进行微波,反应过程中向反应物中滴加二氯亚砜,反应取出后处理得到N-(4-吡啶基)吡啶盐酸盐;将N-(4-吡啶基)吡啶盐酸盐与水混合加热,加入碱性物质调节pH值为7.5-8.5,有沉淀析出,过滤再用酸性物质调节pH值为4.5-5,后处理得到4-吡啶酚。通过上述方式,本发明的4-吡啶酚的制备方法,通过微波方法进行合成,合成过程操作简单,能极大的缩短反应时间,节约生产成本,得到的4-吡啶酚纯度高,副产物几乎没有,不需要进行其他的处理过程,能够直接应用到后续的生产中。
Description
技术领域
本发明涉及精细有机合成领域,特别是涉及一种4-吡啶酚的制备方法。
背景技术
4-吡啶酚的分子式为C5H5NO,分子量为95.1,具有一定的刺激性,对眼睛、呼吸系统和皮肤有很大的刺激作用。4-吡啶酚是一种重要的有机合成中间体,在医药、农药等方面有广泛的用途,能够用于合成利尿药物托拉塞米、治疗充血性心力衰竭药物托洛塞米或其他药物中间体。传统合成4-吡啶酚的过程中会产生大量的副产物,反应时间长。
发明内容
本发明主要解决的技术问题是提供一种4-吡啶酚的制备方法,该方法操作简单且安全可靠。
为解决上述技术问题,本发明采用的一个技术方案是:提供一种4-吡啶酚的制备方法,包括步骤为:
(1)将吡啶和乙酸乙酯混合放入到微波炉中进行微波,反应过程中向反应物中滴加二氯亚砜,反应取出后处理得到N-(4-吡啶基)吡啶盐酸盐;
(2)将N-(4-吡啶基)吡啶盐酸盐与水混合加热,加入碱性物质调节pH值为7.5-8.5,有沉淀析出,过滤再用酸性物质调节pH值为4.5-5,后处理得到4-吡啶酚。
在本发明一个较佳实施例中,步骤(1)中将所述微波炉的温度设置为70-80℃。
在本发明一个较佳实施例中,步骤(1)中所述反应时间为20-30℃。
在本发明一个较佳实施例中,步骤(2)中所述碱性物质为氢氧化钾或氢氧化钠,所述酸性物质为盐酸或硫酸。
本发明的有益效果是:本发明的4-吡啶酚的制备方法,通过微波方法进行合成,合成过程操作简单,能极大的缩短反应时间,节约生产成本,得到的4-吡啶酚纯度高,副产物几乎没有,不需要进行其他的处理过程,能够直接应用到后续的生产中。
具体实施方式
下面将对本发明实施例中的技术方案进行清楚、完整地描述,显然,所描述的实施例仅是本发明的一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其它实施例,都属于本发明保护的范围。
实施例一:
提供一种4-吡啶酚的制备方法,包括步骤为:
(1)将吡啶和乙酸乙酯混合放入到微波炉中进行微波,所述微波炉的温度设置为76℃,反应过程中向反应物中滴加二氯亚砜,所述反应时间为20℃,反应取出后处理得到N-(4-吡啶基)吡啶盐酸盐;
(2)将N-(4-吡啶基)吡啶盐酸盐与水混合加热,加入氢氧化钾或氢氧化钠调节pH值为8.5,有沉淀析出,过滤再用硫酸调节pH值为4.5,后处理得到4-吡啶酚。
实施例二:
提供一种4-吡啶酚的制备方法,包括步骤为:
(1)将吡啶和乙酸乙酯混合放入到微波炉中进行微波,所述微波炉的温度设置为70℃,反应过程中向反应物中滴加二氯亚砜,所述反应时间为30℃,反应取出后处理得到N-(4-吡啶基)吡啶盐酸盐;
(2)将N-(4-吡啶基)吡啶盐酸盐与水混合加热,加入氢氧化钾或氢氧化钠调节pH值为8,有沉淀析出,过滤再用硫酸调节pH值为4.8,后处理得到4-吡啶酚。
实施例三:
提供一种4-吡啶酚的制备方法,包括步骤为:
(1)将吡啶和乙酸乙酯混合放入到微波炉中进行微波,所述微波炉的温度设置为80℃,反应过程中向反应物中滴加二氯亚砜,所述反应时间为27℃,反应取出后处理得到N-(4-吡啶基)吡啶盐酸盐;
(2)将N-(4-吡啶基)吡啶盐酸盐与水混合加热,加入氢氧化钾或氢氧化钠调节pH值为7.5,有沉淀析出,过滤再用盐酸调节pH值为5,后处理得到4-吡啶酚。
以上所述仅为本发明的实施例,并非因此限制本发明的专利范围,凡是利用本发明说明书内容所作的等效结构或等效流程变换,或直接或间接运用在其它相关的技术领域,均同理包括在本发明的专利保护范围内。
Claims (4)
1.一种4-吡啶酚的制备方法,其特征在于,包括步骤为:
(1)将吡啶和乙酸乙酯混合放入到微波炉中进行微波,反应过程中向反应物中滴加二氯亚砜,反应取出后处理得到N-(4-吡啶基)吡啶盐酸盐;
(2)将N-(4-吡啶基)吡啶盐酸盐与水混合加热,加入碱性物质调节pH值为7.5-8.5,有沉淀析出,过滤再用酸性物质调节pH值为4.5-5,后处理得到4-吡啶酚。
2.根据权利要求1所述的4-吡啶酚的制备方法,其特征在于,步骤(1)中将所述微波炉的温度设置为70-80℃。
3.根据权利要求1所述的4-吡啶酚的制备方法,其特征在于,步骤(1)中所述反应时间为20-30℃。
4.根据权利要求1所述的4-吡啶酚的制备方法,其特征在于,步骤(2)中所述碱性物质为氢氧化钾或氢氧化钠,所述酸性物质为盐酸或硫酸。
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995007892A1 (de) * | 1993-09-14 | 1995-03-23 | Hoechst Schering Agrevo Gmbh | Substituierte pyridine, verfahren zu ihrer herstellung und ihre verwendung als schädlingsbekämpfungsmittel und fungizide |
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US5723450A (en) * | 1993-09-14 | 1998-03-03 | Hoechst Schering Agrevo Gmbh | Substituted pyridines, their preparation, and their use as pesticides and fungicides |
CN1468055A (zh) * | 2000-10-03 | 2004-01-14 | �����ɷ� | 苯基丙炔基羟吡啶除草剂 |
CN1560036A (zh) * | 2004-03-12 | 2005-01-05 | 南通市东昌化工有限公司 | 4-羟基吡啶及生产方法 |
CN102947270A (zh) * | 2010-06-22 | 2013-02-27 | 巴斯夫欧洲公司 | 制备4-羟基吡啶的方法 |
-
2013
- 2013-12-06 CN CN201310646586.4A patent/CN103664761A/zh active Pending
Patent Citations (6)
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---|---|---|---|---|
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Title |
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