KR970010725A - Method for preparing polyhydroxy benzophenone - Google Patents

Method for preparing polyhydroxy benzophenone Download PDF

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Publication number
KR970010725A
KR970010725A KR1019950024815A KR19950024815A KR970010725A KR 970010725 A KR970010725 A KR 970010725A KR 1019950024815 A KR1019950024815 A KR 1019950024815A KR 19950024815 A KR19950024815 A KR 19950024815A KR 970010725 A KR970010725 A KR 970010725A
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South Korea
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general formula
solvent
solution
group
preparing
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KR1019950024815A
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Korean (ko)
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KR0153590B1 (en
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김기석
김왕석
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이웅열
주식회사 코오롱
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/29Saturated compounds containing keto groups bound to rings
    • C07C49/337Saturated compounds containing keto groups bound to rings containing hydroxy groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

하기한 일반식(II)와 (III)을 염화알루미늄 또는 염화아연 존재하에서 용매로는 클로로포름, 디클로로에탄, 아세토니트릴, 크실렌 등을 사용하여 구조식(IV) 화합물을 제조하고, 이를 염화알루미늄 또는 시안화나트륨과 반응시켜 구조식(I)의 화합물을 제조하는 폴리히드록시 벤조페논의 제조방법은 매우 높은 수율과 고순도의 제품을 얻을 수 있으며 또한 선택적으로 메톡시기를 히드록시기로 바꿀 수 있는 새로운 폴리히드록시 벤조페논 유도체의 제조방법이다.The following general formulas (II) and (III) are prepared in the presence of aluminum chloride or zinc chloride to prepare a compound of formula (IV) using chloroform, dichloroethane, acetonitrile, xylene, and the like, which are aluminum chloride or sodium cyanide. The process for preparing polyhydroxy benzophenone, which reacts with the compound of formula (I), yields a very high yield and a high purity product, and also a novel polyhydroxy benzophenone derivative capable of selectively converting a methoxy group to a hydroxy group. It is a manufacturing method of.

(식중 R3및 R4는 메틸기 또는 에틸기이며, R1, R2, n, m은 앞에서 정의한 바와 같다.)(Wherein R 3 and R 4 are methyl or ethyl groups and R 1 , R 2 , n, m are as defined above).

Description

폴리히드록시 벤조페논의 제조방법Method for preparing polyhydroxy benzophenone

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음As this is a public information case, the full text was not included.

Claims (7)

하기한 일반식(II)의 메톡시방향족 카르복시산과 하기한 일반식(III)의 메톡시벤젠을 용매에 용해하고 혼합하여 혼합용액을 제조하는 공정과 ; 염화알루미늄 또는 염화아연으로 이루어진 군에서 선택되는 화합물을 용매에 현탁하여 현탁용액을 제조하는 공정과 ; 상기한 혼합용액에 상기한 현탁용액을 첨가하여 반응시켜 하기한 일반식(IV)의 벤조페논 유도체를 제조하는 공정과 ; 상기 벤조페논 유도체에 염화알루미늄 용액을 첨가하여 반응시키는 공정을 ; 포함하는 하기한 일반식(I)의 디히드록시 디메톡시 벤조페논 유도체의 제조방법.Preparing a mixed solution by dissolving and mixing the following methoxyaromatic carboxylic acid of the general formula (II) and the methoxybenzene of the general formula (III) below in a solvent; Preparing a suspension solution by suspending a compound selected from the group consisting of aluminum chloride or zinc chloride in a solvent; Adding the above-mentioned suspension solution to the above-mentioned mixed solution and reacting to prepare a benzophenone derivative of the general formula (IV) shown below; Adding a aluminum chloride solution to the benzophenone derivative to react the reaction; The manufacturing method of the dihydroxy dimethoxy benzophenone derivative of the following general formula (I) containing. (상기 식중 R1, R2는 각각 독립적으로 메틸기 또는 수소이며, R3, 및 R4는 각각 독립적으로 메틸기 또는 에틸기이고 m 및 n은 각각 같거나 다르며 0∼3의 정수이다.)(Wherein R 1 , R 2 are each independently a methyl group or hydrogen, R 3 , and R 4 are each independently a methyl group or an ethyl group, m and n are each the same or different and are integers from 0 to 3). 제1항에 있어서, 상기한 용매는 클로로포름, 디클로로에탄, 아세토니트릴, 크실렌으로 이루어진 군에서 선택되는 것인 제조방법.The method of claim 1, wherein the solvent is selected from the group consisting of chloroform, dichloroethane, acetonitrile and xylene. 제1항에 있어서, 상기한 염화알루미늄 용액의 용매는 디클로로에탄인 제조방법.The method of claim 1, wherein the solvent of the aluminum chloride solution is dichloroethane. 하기한 일반식(II)의 메톡시방향족 카르복시산과 하기한 일반식(III)의 메톡시벤젠을 용매에 용해하고 혼합하여 혼합용액을 제조하는 공정과 ; 염화알루미늄 또는 염화아연으로 이루어진 군에서 선택되는 혼합물을 용매에 현탁하여 현탁용액을 제조하는 공정과 ; 상기한 혼합용액에 상기한 현탁용액을 첨가하여 반응시켜 하기한 일반식(IV)의 벤조페논 유도체를 제조하는 공정과 ; 상기 벤조페논 유도체에 시안화나트륨 용액을 첨가하여 반응시키는 공정을 ; 포함하는 하기한 일반식(V)의 테트라히드록시 벤조페논 유도체의 제조방법.Preparing a mixed solution by dissolving and mixing the following methoxyaromatic carboxylic acid of the general formula (II) and the methoxybenzene of the general formula (III) below in a solvent; Preparing a suspension solution by suspending a mixture selected from the group consisting of aluminum chloride or zinc chloride in a solvent; Adding the above-mentioned suspension solution to the above-mentioned mixed solution and reacting to prepare a benzophenone derivative of the general formula (IV) shown below; Reacting the benzophenone derivative by adding sodium cyanide solution; The manufacturing method of the tetrahydroxy benzophenone derivative of the following general formula (V) containing. (상기 식 중 R1, R2는 각각 독립적으로 메틸기 또는 수소이며, R3및 R4는 각각 독립적으로 메틸기 또는 에틸기이고 m 및 n은 각각 같거나 다르며 0∼3의 정수이다.)(Wherein R 1 and R 2 are each independently a methyl group or hydrogen, R 3 and R 4 are each independently a methyl group or an ethyl group and m and n are each the same or different and are an integer from 0 to 3). 제4항에 있어서, 상기한 용매는 클로로포름, 디클로로에탄, 아세토니트릴, 크실렌으로 이루어진 군에서 선택되는 것인 제조방법.The method according to claim 4, wherein the solvent is selected from the group consisting of chloroform, dichloroethane, acetonitrile and xylene. 제4항에 있어서, 상기한 시안화나트륨 용액의 용매는 디메틸설폭사이드인 제조방법.The method of claim 4, wherein the solvent of the sodium cyanide solution is dimethyl sulfoxide. 하기한 일반식(II)의 메톡시방향족 카르복시산과 하기한 일반식(III)의 메톡시벤젠을 용매에 용해하고 혼합하여 혼합용액을 제조하는 공정과 ; 염화알루미늄 또는 염화아연으로 이루어진 군에서 선택되는 혼합물을 용매에 현탁하여 현탁용액을 제조하는 공정과 ; 상기한 혼합용액에 상기한 현탁용액을 첨가하여 반응시키는 공정을 ; 포함하는 하기한 일반식(IV)의 벤조페논 유도체의 제조방법.Preparing a mixed solution by dissolving and mixing the following methoxyaromatic carboxylic acid of the general formula (II) and the methoxybenzene of the general formula (III) below in a solvent; Preparing a suspension solution by suspending a mixture selected from the group consisting of aluminum chloride or zinc chloride in a solvent; Adding a suspension solution to the mixed solution and reacting the same; The manufacturing method of the benzophenone derivative of the following general formula (IV) containing. (상기 식 중 R1,R2는 각각 독립적으로 메틸기 또는 수소이며, R3및 R4는 각각 독립적으로 메틸기 또는 에틸기이고 m 및 n은 각각 같거나 다르며 0∼3의 정수이다.)(Wherein R 1 and R 2 are each independently a methyl group or hydrogen, R 3 and R 4 are each independently a methyl group or an ethyl group and m and n are the same or different and are integers of 0 to 3). ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019950024815A 1995-08-11 1995-08-11 Process for producing polyhydroxybenzophenone KR0153590B1 (en)

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KR0153590B1 KR0153590B1 (en) 1998-12-01

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100426394B1 (en) * 2001-10-26 2004-04-08 엘지전선 주식회사 The controlling method and device of deposition paricle in farbricating large preform by outside vapor deposition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100426394B1 (en) * 2001-10-26 2004-04-08 엘지전선 주식회사 The controlling method and device of deposition paricle in farbricating large preform by outside vapor deposition

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