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RU2012119099A - METHOD FOR PRODUCING COMPOUND ETHER OF MONOCHLOROUS ACID CONTAINING 1,3-DIOXANE SUBSTITUTE - Google Patents

METHOD FOR PRODUCING COMPOUND ETHER OF MONOCHLOROUS ACID CONTAINING 1,3-DIOXANE SUBSTITUTE Download PDF

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Publication number
RU2012119099A
RU2012119099A RU2012119099/04A RU2012119099A RU2012119099A RU 2012119099 A RU2012119099 A RU 2012119099A RU 2012119099/04 A RU2012119099/04 A RU 2012119099/04A RU 2012119099 A RU2012119099 A RU 2012119099A RU 2012119099 A RU2012119099 A RU 2012119099A
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RU
Russia
Prior art keywords
dioxane
ethyl
hydroxymethyl
monochlorous
substitute
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RU2012119099/04A
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Russian (ru)
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RU2503670C1 (en
Inventor
Семён Соломонович Злотский
Эльвира Хамзовна Гиниятуллина
Наталья Николаевна Михайлова
Анна Александровна Богомазова
Original Assignee
Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Уфимский государственный нефтяной технический университет"
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Priority to RU2012119099/04A priority Critical patent/RU2503670C1/en
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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

1. Способ получения сложного эфира монохлоруксусной кислоты, содержащего 1,3-диоксановый заместитель, переэтерификацией этилового эфира монохлоруксусной кислоты 5-этил-5-гидроксиметил-1,3-диоксаном проводят в присутствии Purolite CT 275 в качестве катализатора при температуре 90-100°C в течение 3-3,5 ч.2. Способ по п.1, отличающийся тем, что реакцию с 5-этил-5-гидроксиметил-1,3-диоксаном проводят при следующем соотношении компонентов, мас.%: этилового эфира монохлоруксусной кислоты 60-63; 5-этил-5-гидроксиметил-1,3-диоксана 30-32.3. Способ по п.1, отличающийся тем, что используют катализатор Purolite CT 275 в количестве 7-8 мас.% от 5-этил-5-гидроксиметил-1,3-диоксана.1. A method for producing a monochloracetic acid ester containing a 1,3-dioxane substituent by transesterification of the monochloracetic acid ethyl ester with 5-ethyl-5-hydroxymethyl-1,3-dioxane is carried out in the presence of Purolite CT 275 as a catalyst at a temperature of 90-100 ° C for 3-3.5 hours. 2. The method according to claim 1, characterized in that the reaction with 5-ethyl-5-hydroxymethyl-1,3-dioxane is carried out in the following ratio of components, wt.%: Monochloracetic acid ethyl ester 60-63; 5-ethyl-5-hydroxymethyl-1,3-dioxane 30-32.3. The method according to claim 1, characterized in that they use a Purolite CT 275 catalyst in an amount of 7-8 wt.% From 5-ethyl-5-hydroxymethyl-1,3-dioxane.

Claims (3)

1. Способ получения сложного эфира монохлоруксусной кислоты, содержащего 1,3-диоксановый заместитель, переэтерификацией этилового эфира монохлоруксусной кислоты 5-этил-5-гидроксиметил-1,3-диоксаном проводят в присутствии Purolite CT 275 в качестве катализатора при температуре 90-100°C в течение 3-3,5 ч.1. A method for producing a monochloracetic acid ester containing a 1,3-dioxane substituent by transesterification of the monochloracetic acid ethyl ester with 5-ethyl-5-hydroxymethyl-1,3-dioxane is carried out in the presence of Purolite CT 275 as a catalyst at a temperature of 90-100 ° C for 3-3.5 hours 2. Способ по п.1, отличающийся тем, что реакцию с 5-этил-5-гидроксиметил-1,3-диоксаном проводят при следующем соотношении компонентов, мас.%: этилового эфира монохлоруксусной кислоты 60-63; 5-этил-5-гидроксиметил-1,3-диоксана 30-32.2. The method according to claim 1, characterized in that the reaction with 5-ethyl-5-hydroxymethyl-1,3-dioxane is carried out in the following ratio of components, wt.%: Monochloracetic acid ethyl ester 60-63; 5-ethyl-5-hydroxymethyl-1,3-dioxane 30-32. 3. Способ по п.1, отличающийся тем, что используют катализатор Purolite CT 275 в количестве 7-8 мас.% от 5-этил-5-гидроксиметил-1,3-диоксана. 3. The method according to claim 1, characterized in that they use a Purolite CT 275 catalyst in an amount of 7-8 wt.% From 5-ethyl-5-hydroxymethyl-1,3-dioxane.
RU2012119099/04A 2012-05-10 2012-05-10 Method of producing monochloroacetic acid ester containing 1,3-dioxane substitute RU2503670C1 (en)

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RU2012119099/04A RU2503670C1 (en) 2012-05-10 2012-05-10 Method of producing monochloroacetic acid ester containing 1,3-dioxane substitute

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RU2012119099/04A RU2503670C1 (en) 2012-05-10 2012-05-10 Method of producing monochloroacetic acid ester containing 1,3-dioxane substitute

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RU2012119099A true RU2012119099A (en) 2013-11-20
RU2503670C1 RU2503670C1 (en) 2014-01-10

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Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1493572A1 (en) * 1965-12-02 1969-11-13 Huels Chemische Werke Ag Process for the preparation of cycloacetal and cycloketal esters
RU2098404C1 (en) * 1995-06-06 1997-12-10 Акционерное общество открытого типа "Кирово-Чепецкий химический комбинат им.Б.П.Константинова" Method of synthesis of monochloroacetic acid methyl ester

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Effective date: 20140511