KR19990027763A - Method for preparing ο- (chloromethyl) benzoic acid ester derivative - Google Patents
Method for preparing ο- (chloromethyl) benzoic acid ester derivative Download PDFInfo
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- KR19990027763A KR19990027763A KR1019970050284A KR19970050284A KR19990027763A KR 19990027763 A KR19990027763 A KR 19990027763A KR 1019970050284 A KR1019970050284 A KR 1019970050284A KR 19970050284 A KR19970050284 A KR 19970050284A KR 19990027763 A KR19990027763 A KR 19990027763A
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- C07C67/00—Preparation of carboxylic acid esters
- C07C67/14—Preparation of carboxylic acid esters from carboxylic acid halides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
Abstract
본 발명은o-(클로로메틸)벤조산 에스테르 유도체의 제조방법에 관한 것으로서, 더욱 상세하게는o-(클로로메틸)벤조산 클로라이드를 출발물질로 하고 알콜화합물을 반응물질 및 반응용매로 사용하여 보다 간편한 조작과 온화한 조건하에서 에스테르화 반응시키므로써 작물보호제를 합성하는 중요한 중간체 화합물인 다음 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체를 제조하는 새로운 방법에 관한 것이다.The present invention relates to a method for preparing o- (chloromethyl) benzoic acid ester derivative, and more particularly, simple operation by using o- (chloromethyl) benzoic acid chloride as a starting material and an alcohol compound as a reactant and a reaction solvent. The present invention relates to a novel process for preparing o- (chloromethyl) benzoic acid ester derivative represented by the following Chemical Formula 1, which is an important intermediate compound for synthesizing crop protection agents by esterification under mild conditions.
상기 화학식 1에서: R1은 수소원자, 할로겐원자, C1∼ C6의 알킬기, C1∼ C6의 할로알킬기, C1∼ C6의 알콕시기, C1∼ C6의 알콕시카르보닐기, 니트로기 또는 페닐기를 나타내고; R2는 C1∼ C6의 알킬기, C1∼ C6의 할로알킬기 또는 C3∼ C6의 사이클로알킬기를 나타낸다.In the general formula 1: R 1 is an alkoxycarbonyl group, a nitro a hydrogen atom, a halogen atom, C 1 ~ C 6 alkyl group, C 1 ~ C 6 haloalkyl group, C 1 ~ C 6 alkoxy group, C 1 ~ C 6 of the Group or phenyl group; R 2 represents a cycloalkyl group of C 1 ~ C 6 alkyl group, C 1 ~ C 6 haloalkyl group or a C 3 ~ C 6 of the.
Description
본 발명은o-(클로로메틸)벤조산 클로라이드를 출발물질로 하고 알콜화합물을 반응물질 및 반응용매로 사용하여 보다 간편한 조작과 온화한 조건하에서 에스테르화 반응시키므로써 작물보호제를 합성하는 중요한 중간체 화합물인 다음 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체를 제조하는 새로운 방법에 관한 것이다.The present invention is an important intermediate compound for synthesizing a crop protection agent by using o- (chloromethyl) benzoic acid chloride as a starting material and an alcohol compound as a reactant and a reaction solvent to make esterification under simpler operation and mild conditions. It relates to a new method for preparing the o- (chloromethyl) benzoic acid ester derivative represented by 1.
화학식 1Formula 1
상기 화학식 1에서: R1은 수소원자, 할로겐원자, C1∼ C6의 알킬기, C1∼ C6의 할로알킬기, C1∼ C6의 알콕시기, C1∼ C6의 알콕시카르보닐기, 니트로기 또는 페닐기를 나타내고; R2는 C1∼ C6의 알킬기, C1∼ C6의 할로알킬기 또는 C3∼ C6의 사이클로알킬기를 나타낸다.In the general formula 1: R 1 is an alkoxycarbonyl group, a nitro a hydrogen atom, a halogen atom, C 1 ~ C 6 alkyl group, C 1 ~ C 6 haloalkyl group, C 1 ~ C 6 alkoxy group, C 1 ~ C 6 of the Group or phenyl group; R 2 represents a cycloalkyl group of C 1 ~ C 6 alkyl group, C 1 ~ C 6 haloalkyl group or a C 3 ~ C 6 of the.
상기 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체는 작물보호제를 합성하는 중요한 중간체 화합물로서 공지되어있다[미국특허 제4,420,325호; 중국논문 Hauxue Shijie 31 , 211(1990)].The o- (chloromethyl) benzoic acid ester derivative represented by the above formula (1) is known as an important intermediate compound for synthesizing crop protection agents [US Pat. No. 4,420,325; Chinese paper Hauxue Shijie 31 , 211 (1990)].
상기 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체를 합성하는 종래의 방법으로서, 미국특허 제4,689,425호에는o-메틸벤조산 메틸 에스테르의 곁가지 메틸기에 UV 빛을 쬐이면서 염소가스와 염화수소가스를 주입하여 염소화반응을 시켜o-(클로로메틸)벤조산 메틸 에스테르를 제조하는 방법이 게시되어 있다. 그러나 이 방법은 출발물질이 10% 정도 남은 상태에서 반응을 종료시켜도 부생성물이 많이 생기기 때문에 목적물의 분리공정이 까다롭고 제조수율도 크게 떨어지며, 또 출발물질이 모두 없어지도록 반응을 진행시키면 부생성물의 양은 더 많아지고 수율도 크게 떨어진다.As a conventional method for synthesizing o- (chloromethyl) benzoic acid ester derivative represented by Chemical Formula 1, US Pat. No. 4,689,425 discloses chlorine gas and hydrogen chloride gas while exposing UV light to a side methyl group of o -methylbenzoic acid methyl ester. A method of preparing o- (chloromethyl) benzoic acid methyl ester by injecting by chlorination has been published. However, this method produces many by-products even when the reaction is terminated with about 10% of the starting material remaining. Therefore, the separation process of the target is difficult and the production yield is greatly reduced. More quantities and yields fall significantly.
본 발명은o-(클로로메틸)벤조산 클로라이드를 출발물질로 하고, 간편한 조작과 온화한 조건하에서 알콜화합물을 반응물질 및 반응용매로 사용하여 에스테르화 반응시키므로써 목적으로 하는 상기 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체를 높은 제조수율로 수득하는 방법을 제공하는데 그 목적이 있다. O- present invention represented by the formula (1) for the purpose of writing because o- (chloromethyl) and the acid chloride as a starting material, using the alcohol compound as the reaction materials and the reaction solvent under mild conditions with easy operation Esterification It is an object to provide a method for obtaining (chloromethyl) benzoic acid ester derivative in high production yield.
본 발명은 다음 화학식 2로 표시되는o-(클로로메틸)벤조산 클로라이드와 다음 화학식 3으로 표시되는 알콜화합물을 반응시켜 다음 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체를 제조하는 방법을 그 특징으로 한다.The present invention provides a method for preparing an o- (chloromethyl) benzoic acid ester derivative represented by the following Chemical Formula 1 by reacting an o- (chloromethyl) benzoic acid chloride represented by the following Chemical Formula 2 with an alcohol compound represented by the following Chemical Formula 3. It features.
화학식 1Formula 1
상기 화학식들에서, R1과 R2는 각각 상기에서 정의한 바와 같다.In the above formula, R 1 and R 2 are as defined above, respectively.
본 발명에 따른 상기 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체의 제조방법을 간략히 나타내면 다음 반응식 1과 같다.The preparation method of the o- (chloromethyl) benzoic acid ester derivative represented by Chemical Formula 1 according to the present invention is briefly shown in Scheme 1 below.
상기 반응식에서, R1과 R2는 각각 상기에서 정의한 바와 같다.In the above scheme, R 1 and R 2 are each as defined above.
본 발명에서 출발믈질로 사용하는 상기 화학식 2로 표시되는o-(클로로메틸)벤조산 클로라이드는 공지 화합물로서 공지 제조방법에 의해 쉽게 제조하여 사용할 수 있다[미국특허 제5,504,249호; 유럽특허 제413,264호]The o- (chloromethyl) benzoic acid chloride represented by Chemical Formula 2 used as a starting material in the present invention can be easily prepared and used by a known production method as a known compound [US Patent No. 5,504,249; European Patent No. 413,264]
본 발명에 따른 상기 화학식 2로 표시되는o-(클로로메틸)벤조산 클로라이드와 화학식 3으로 표시되는 알콜화합물과의 에스테르화 반응은 -5 ~ 100℃, 바람직하기로는 40 ∼ 50℃에서 수행한다. 이때, 알콜화합물은 반응용매로서 그리고 반응물질로서 사용되며, 그 사용량에 있어서도 특별한 제한은 없으나 상기 화학식 2로 표시되는o-(클로로메틸)벤조산 클로라이드에 대하여 몰비로 1 ∼ 10당량, 바람직하기로는 1.2 ∼ 1.5 당량 사용하는 것이 경제적이다.The esterification reaction of o- (chloromethyl) benzoic acid chloride represented by Formula 2 according to the present invention with an alcohol compound represented by Formula 3 is carried out at -5 to 100 ° C, preferably at 40 to 50 ° C. At this time, the alcohol compound is used as a reaction solvent and as a reaction material, there is no particular limitation on the amount of use, but 1 to 10 equivalents, preferably 1.2, in molar ratio with respect to the o- (chloromethyl) benzoic acid chloride represented by the formula (2). It is economical to use 1.5 equivalents.
본 발명에 따른 에스테르화 반응은 염기가 첨가되지 않아도 반응은 온화하게 진행되나, 염기로서 3차아민 예를들면 트리메틸아민, 트리에틸아민, 트리이소프로필아민 등의 알킬아민이나 피리딘 등의 방향족 아민화합물을 첨가하게되면 보다 온화한 존건하에서 높은 제조수율로 목적물을 얻을 수 있다. 에스테르화반응시 염기가 첨가된 경우, 반응온도는 0 ∼ 20℃ 바람직하기로는 5 ∼ 10℃를 유지한다.In the esterification reaction according to the present invention, the reaction proceeds mildly even if no base is added. When added, the target product can be obtained with high production yield under milder condition. When a base is added during the esterification reaction, the reaction temperature is maintained at 0 to 20 ° C, preferably 5 to 10 ° C.
상기와 같은 조건하에서 에스테르화 반응이 완결되면 통상의 정제방법으로 목적물을 회수하는데, 예를들면 반응 혼합물을 물로 세척한 후에 분별감압증류를 하거나 또는 세척과정을 거치지 않고 곧바로 반응 혼합물을 분별감압증류한다.Under the above conditions, when the esterification reaction is completed, the target product is recovered by a conventional purification method.For example, the reaction mixture is washed with water and then subjected to fractional distillation or the reaction mixture is subjected to fractional distillation immediately without washing. .
이하 본 발명을 다음의 실시예에 의거하여 더욱 상세히 설명하는 바, 본 발명이 실시예에 한정되는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to the following examples, but the present invention is not limited to the examples.
실시예 1 :Example 1: o-o- (클로로메틸)벤조산 메틸 에스테르의 합성Synthesis of (chloromethyl) benzoic acid methyl ester
냉각기, 온도계 그리고 드롭핑 펀넬(dropping funnel)이 장치된 500㎖ 2구 플라스크에o-(클로로메틸)벤조산 클로라이드 180g을 넣고, 내부온도를 40 ∼ 50℃로 유지하면서 메탄올 50㎖를 서서히 적하하였다. 메탄올이 모두 적하되면, 반응기 내부온도를 40 ∼ 50℃로 유지하면서 10시간 교반하였다. 곧바로 증류기를 장치하여 분별감압증류하여 목적화합물 165g(수율 94%)을 오일로 얻었다.180 g of o- (chloromethyl) benzoic acid chloride was placed in a 500 ml two-necked flask equipped with a cooler, a thermometer, and a dropping funnel, and 50 ml of methanol was slowly added dropwise while maintaining an internal temperature of 40 to 50 ° C. When all the methanol was dripped, it stirred for 10 hours, keeping reactor internal temperature at 40-50 degreeC. Immediately distillation was carried out in a distillation apparatus to give 165 g (yield 94%) of the title compound as an oil.
끓는점 : 77 ∼ 80℃(1 mmHg)Boiling Point: 77∼80 ℃ (1 mmHg)
1H-NMR(CDCl3) : δ3.9(s, 3H), 5.02(s, 2H), 7.31∼7.56(m, 3H), 7.96(d, 1H,J=8Hz) 1 H-NMR (CDCl 3 ): δ 3.9 (s, 3H), 5.02 (s, 2H), 7.31-7.56 (m, 3H), 7.96 (d, 1H, J = 8 Hz)
실시예 2 :Example 2: o-o- (클로로메틸)벤조산 메틸 에스테르의 합성Synthesis of (chloromethyl) benzoic acid methyl ester
냉각기, 온도계 그리고 드롭핑 펀넬(dropping funnel)이 장치된 500㎖ 2구 플라스크에o-(클로로메틸)벤조산 클로라이드 180g을 1000㎖의 염화메틸렌에 녹이고 반응액의 내부온도를 0℃로하여 트리에틸아민(138㎖)을 넣고 메탄올 50㎖를 서서히 적하하였다. 메탄올이 모두 적하되면, 반응기 내부온도를 20 ∼ 30℃로 유지하면서 10시간 교반하였다. 반능액을 5% 염산용액 300㎖로 세척하고 유기층을 분리하여 황산 마그네슘으로 건조하고,여과 농축과정을 거쳐 생성된 여액을 분별감압증류하여 목적화합물 155g(수율 88%)을 오일로 얻었다.Dissolve 180 g of o- (chloromethyl) benzoic acid chloride in 1000 ml of methylene chloride in a 500 ml two-necked flask equipped with a cooler, a thermometer, and a dropping funnel, and triethylamine at an internal temperature of 0 ° C. (138 ml) was added and 50 ml of methanol was slowly added dropwise. When all the methanol was dripped, it stirred for 10 hours, keeping reactor internal temperature at 20-30 degreeC. The reaction solution was washed with 300 ml of 5% hydrochloric acid solution, the organic layer was separated, dried over magnesium sulfate, and the filtrate was concentrated under reduced pressure to give 155 g (yield 88%) of the target compound as an oil.
실시예 3 :Example 3: oo -(클로로메틸)벤조산 에틸 에스테르의 합성Synthesis of-(chloromethyl) benzoic acid ethyl ester
냉각기, 온도계 그리고 드롭핑 펀넬(dropping funnel)이 장치된 500㎖ 2구 플라스크에o-(클로로메틸)벤조산 클로라이드 180g을 넣고, 내부온도를 40 ∼ 50℃로 유지하면서 에탄올 60㎖를 서서히 적하하였다. 에탄올이 모두 적하되면, 반응기 내부온도를 40 ∼ 50℃로 유지하면서 10시간 교반하였다. 곧바로 증류기를 장치하여 분별감압증류하여 목적화합물 179g(수율 90%)을 오일로 얻었다.180 g of o- (chloromethyl) benzoic acid chloride was added to a 500 ml two-necked flask equipped with a cooler, a thermometer, and a dropping funnel, and 60 ml of ethanol was slowly added dropwise while maintaining an internal temperature of 40 to 50 ° C. When all ethanol was dripped, it stirred for 10 hours, keeping reactor internal temperature at 40-50 degreeC. Immediately distillation was carried out in a distillation apparatus to obtain 179 g (yield 90%) of the title compound as an oil.
끓는점 : 79 ∼ 82℃ (1 mmHg)Boiling Point: 79∼82 ℃ (1 mmHg)
1H-NMR(CDCl3) : δ1.4(t, 3H,J=8Hz), 4.38(q, 2H,J=8Hz), 5.02(s, 2H), 7.32∼ 7.55(m, 3H), 7.96(d, 1H,J=8Hz) 1 H-NMR (CDCl 3 ): δ 1.4 (t, 3H, J = 8 Hz), 4.38 (q, 2H, J = 8 Hz), 5.02 (s, 2H), 7.32 to 7.55 (m, 3H), 7.96 (d, 1H, J = 8 Hz)
실시예 4 :Example 4: oo -(클로로메틸)벤조산 2-클로로에틸 에스테르의 합성Synthesis of-(chloromethyl) benzoic acid 2-chloroethyl ester
냉각기, 온도계 그리고 드롭핑 펀넬(dropping funnel)이 장치된 500㎖ 2구 플라스크에o-(클로로메틸)벤조산 클로라이드 180g을 넣고, 내부온도를 40 ∼ 50℃로 유지하면서 2-클로로에탄올 50㎖를 서서히 적하하였다. 2-클로로에탄올이 모두 적하되면, 반응기 내부온도를 40 ∼ 50℃로 유지하면서 10시간 교반하였다. 곧바로 증류기를 장치하여 분별감압증류하여 목적화합물 165g(수율 94%)을 오일로 얻었다.180 g of o- (chloromethyl) benzoic acid chloride was added to a 500 ml two-necked flask equipped with a cooler, a thermometer, and a dropping funnel, and 50 ml of 2-chloroethanol was slowly added while maintaining an internal temperature of 40 to 50 ° C. It dripped. When all 2-chloroethanol was dripped, it stirred for 10 hours, keeping reactor internal temperature at 40-50 degreeC. Immediately distillation was carried out in a distillation apparatus to give 165 g (yield 94%) of the title compound as an oil.
끓는점 : 88 ∼ 92℃(1.1 mmHg)Boiling Point: 88∼92 ℃ (1.1 mmHg)
1H-NMR(CDCl3) : δ3.83(t, 2H,J=5.5Hz) 4.59(t, 2H,J=5.5Hz), 5.02(s, 2H), 7.36 ∼7.58(m, 3H), 8.01(d, 1H,J=8Hz) 1 H-NMR (CDCl 3 ): δ3.83 (t, 2H, J = 5.5 Hz) 4.59 (t, 2H, J = 5.5 Hz), 5.02 (s, 2H), 7.36-7.58 (m, 3H), 8.01 (d, 1H, J = 8 Hz)
본 발명에 따른 제조방법은 온화한 반응조건하에서 수행되므로 상기 화학식 1로 표시되는o-(클로로메틸)벤조산 에스테르 유도체의 공업적인 생산에 유용하다.Since the preparation method according to the present invention is carried out under mild reaction conditions, it is useful for industrial production of o- (chloromethyl) benzoic acid ester derivative represented by Chemical Formula 1.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019970050284A KR100252462B1 (en) | 1997-09-30 | 1997-09-30 | Process for prparing o-(chloromethyl)benzoic acid ester derivatives |
| CN98809695A CN1120149C (en) | 1997-09-30 | 1998-09-30 | Process for preparing i(O)-(carboalkoxy) phenylmethanesulfonyl chloride derivatives |
| PCT/KR1998/000302 WO1999016743A1 (en) | 1997-09-30 | 1998-09-30 | A PROCESS FOR PREPARING o-(CARBOALKOXY) PHENYLMETHANESULFONYL CHLORIDE DERIVATIVES |
| JP2000513829A JP3433319B2 (en) | 1997-09-30 | 1998-09-30 | Method for producing o- (carboalkoxy) phenylmethanesulfonyl derivative |
| US09/509,440 US6222060B1 (en) | 1997-09-30 | 2000-03-28 | Process for preparing o-(carboalkoxy)phenylmethanesulfonyl chloride derivatives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1019970050284A KR100252462B1 (en) | 1997-09-30 | 1997-09-30 | Process for prparing o-(chloromethyl)benzoic acid ester derivatives |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR19990027763A true KR19990027763A (en) | 1999-04-15 |
| KR100252462B1 KR100252462B1 (en) | 2000-04-15 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019970050284A KR100252462B1 (en) | 1997-09-30 | 1997-09-30 | Process for prparing o-(chloromethyl)benzoic acid ester derivatives |
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| Country | Link |
|---|---|
| KR (1) | KR100252462B1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100347137B1 (en) * | 1999-12-27 | 2002-07-31 | 주식회사 하이닉스반도체 | Inhibitor device for accumulating impurity in exhausting pipe |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3382423B2 (en) * | 1995-07-31 | 2003-03-04 | ジャパンエポキシレジン株式会社 | Method for esterifying phenolic compounds |
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1997
- 1997-09-30 KR KR1019970050284A patent/KR100252462B1/en not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100347137B1 (en) * | 1999-12-27 | 2002-07-31 | 주식회사 하이닉스반도체 | Inhibitor device for accumulating impurity in exhausting pipe |
Also Published As
| Publication number | Publication date |
|---|---|
| KR100252462B1 (en) | 2000-04-15 |
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