SU143397A1 - The method of obtaining merkur-bis-acetaldehyde - Google Patents

The method of obtaining merkur-bis-acetaldehyde

Info

Publication number
SU143397A1
SU143397A1 SU722124A SU722124A SU143397A1 SU 143397 A1 SU143397 A1 SU 143397A1 SU 722124 A SU722124 A SU 722124A SU 722124 A SU722124 A SU 722124A SU 143397 A1 SU143397 A1 SU 143397A1
Authority
SU
USSR - Soviet Union
Prior art keywords
bis
acetaldehyde
merkur
obtaining
oxide
Prior art date
Application number
SU722124A
Other languages
Russian (ru)
Inventor
А.И. Балин
Т.Н. Веретенова
Original Assignee
А.И. Балин
Т.Н. Веретенова
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by А.И. Балин, Т.Н. Веретенова filed Critical А.И. Балин
Priority to SU722124A priority Critical patent/SU143397A1/en
Application granted granted Critical
Publication of SU143397A1 publication Critical patent/SU143397A1/en

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  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Известен-способ получени  меркур-бис-ацетальдегнда взанмодействием простого винилового эфира с желтой окисью ртути и ацетатом ртути.A known method for the preparation of merkur-bis-acetaldegnd is by the reaction of vinyl ether with yellow oxide of mercury and mercury acetate.

Пред.тагаетс  способ получени  меркур-бис-ацетальдегида взаимодействием дивинилацетал  с желтой окисью .ртути в присутствии ацетата ртути в инертном растворителе.A method for the preparation of mercurice bis acetaldehyde by the interaction of divinyl acetal with yellow mercury oxide in the presence of mercury acetate in an inert solvent is suggested.

Получение, меркур-бис-ацетальдегида из дивинилацетал  и окиси ртути в литературе не описано.The preparation of mercuris bis acetaldehyde from divinylacetal and mercuric oxide has not been described in the literature.

Способ базируетс  на доступном сырье, достаточно прост и безопасен , обеспечивает хороший выход целевого продукта, который дгожет найти применение в синтезе виниловых бифункциональных мономеров.The method is based on available raw materials, is quite simple and safe, provides a good yield of the target product, which can be used in the synthesis of vinyl bifunctional monomers.

Пример. К смеси 21,6 г (0,1 мол ) желтой окиси ртути, 0,8 , (0,0025 мол ) уксуснокислой ги, 4 мл волы и 8 мл спирта прибавл ют по капл м при пере-мешиванин 14,2 г (0,1 мол ) дивин1 лбут1;рал . Окись ртути с разогревание.м раствор етс . Реакционную с.месь в теплом состо нии отфильтровывают от следов ртути и сильно охлаж-.Example. To a mixture of 21.6 g (0.1 mol) of yellow mercuric oxide, 0.8, (0.0025 mol) of acetic acid gi, 4 ml of oxen and 8 ml of alcohol is added dropwise with a 14.2 g mixed ( 0.1 mol) divin1 lbut1; ral. The mercuric oxide with reheating.m dissolves. The reaction mixture is heated in a warm state from traces of mercury and strongly cooled.

дают. Выпавшие кристаллы отдел ют, прол.ывают холодным спиртом ... j и эфиро.м. Выход сухого меркур-бис-ацетальдегида-24,8 г (85% от give. The precipitated crystals are separated, proled with cold alcohol ... j and ether. The yield of dry mercuris bis-acetaldehyde is 24.8 g (85% of

теоретического). Константы полученного продукта хорошо совпадп.-отjtheoretical). The constants of the product obtained are well-matched.

с указанными в литературе.|with those listed in the literature. |

В случае возникноиени  потребности в меркур-бис-ацетальдегиле способ может быть использован в промышленности.. .In case of a need for merkur-bis-acetaldegile, the method can be used in industry ...

П ре д м ет из об р.ет е и и  It is made of

Способ получени  меркур-бис-ацетальдегида из окиси ргути и иинилового эфира в присутствии ацетата ртути, отличающийс  тем, что в качестве вигшлового эфира примен ют дивинилацеталь.The method of producing mercuric bis-acetaldehyde from rgut oxide and ethyl ether in the presence of mercury acetate, characterized in that divinylacetal is used as the upper ester.

SU722124A 1961-03-17 1961-03-17 The method of obtaining merkur-bis-acetaldehyde SU143397A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU722124A SU143397A1 (en) 1961-03-17 1961-03-17 The method of obtaining merkur-bis-acetaldehyde

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU722124A SU143397A1 (en) 1961-03-17 1961-03-17 The method of obtaining merkur-bis-acetaldehyde

Publications (1)

Publication Number Publication Date
SU143397A1 true SU143397A1 (en) 1961-11-30

Family

ID=48299163

Family Applications (1)

Application Number Title Priority Date Filing Date
SU722124A SU143397A1 (en) 1961-03-17 1961-03-17 The method of obtaining merkur-bis-acetaldehyde

Country Status (1)

Country Link
SU (1) SU143397A1 (en)

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