SU152238A1 - The method of obtaining the acid chloride symmetric tetramethyldiphenyldisiloxanecarboxy- (4,4 ') acid - Google Patents

The method of obtaining the acid chloride symmetric tetramethyldiphenyldisiloxanecarboxy- (4,4 ') acid

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Publication number
SU152238A1
SU152238A1 SU773746A SU773746A SU152238A1 SU 152238 A1 SU152238 A1 SU 152238A1 SU 773746 A SU773746 A SU 773746A SU 773746 A SU773746 A SU 773746A SU 152238 A1 SU152238 A1 SU 152238A1
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SU
USSR - Soviet Union
Prior art keywords
acid
symmetric
acid chloride
obtaining
tetramethyldiphenyldisiloxanecarboxy
Prior art date
Application number
SU773746A
Other languages
Russian (ru)
Inventor
Г.Н. Мальнова
Е.П. Михеев
Original Assignee
Г.Н. Мальнова
Е.П. Михеев
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 Г.Н. Мальнова, Е.П. Михеев filed Critical Г.Н. Мальнова
Priority to SU773746A priority Critical patent/SU152238A1/en
Application granted granted Critical
Publication of SU152238A1 publication Critical patent/SU152238A1/en

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Известен способ получени  хлорангидрида тетраметилдифепилдиСилоксандикарбоновой-{4 ,4) кислоты действнем хлористого тиснила на тетраметилдифенилдисилоксандикарбоновую-(4,4) кислоту с последующей перекристаллизацией полученного продукта и выходом его 47%.A known method for the preparation of tetramethyldipheldyl-siloxane dicarboxylic- {4, 4) acid chloride is actual tisnyl chloride on tetramethyldiphenyl disilyloxane dicarboxylic- (4,4) acid, followed by recrystallization of the obtained product and its yield of 47%.

Предлагаемый способ получени  хлорангидрида симметричной тетраметилдифенилдисилок1санд карбоновой- (4,4) кислоты отличаетс  тем, что хлорангидрид п-(диметилхлорсилил) бензойной кислоты гидролизуют водой при температуре не выше 1°. Способ позвол ет расширить сырьевую базу дл  получени  высокомолекул рных полимеров. The proposed method for preparing a symmetric tetramethyldiphenyl disilicone carbonyl- (4,4) acid chloride is characterized in that the acid chloride of p- (dimethylchlorosilyl) benzoic acid is hydrolyzed with water at a temperature not higher than 1 °. The method allows the raw material base to be expanded to produce high molecular weight polymers.

Полученное соединение может найти широкое применение дл  синтеза различных высокомолекул рных линейных полимеров линейной структуры.The compound obtained can be widely used for the synthesis of various high molecular weight linear polymers of linear structure.

Пример. В стекл нный стакан емк. 1 л, снабженный мешалкой, термометром и капельной воронкой, загружают 500 мл воды. Стакан с .водой охлаждают смесью льда с солью. При достижении в воде температуры 1° при интенсивном перемешивании добавл ют частыми капл ми 106,75 г хлорангидрида п-(диметилхлорсилил) бензойной кислоты. По окончании подачи хлорангидрида содержимое стакана перемешивают в течение 30 мин, после чего быстро перенос т на воронку Бюхнера дл  отделени  кристаллов хлорангидрида тетраметилдифенилдисилоксандикарбоновой- (4,4) кислоты от образовавшейс  сол ной кислоты. Кристаллы на фильтре промывают 3 раза охлажденной до 1° водой, отжимают , затем сразу помещают в вакуум-эксикатор, где высушивают над серной кислотой. Получают 90 г хлорангидрида с т. пл. 54-55° и содертжаннем хлора 17,31%.Example. In a glass glass tank. 1 liter, equipped with a stirrer, a thermometer and a dropping funnel, is charged with 500 ml of water. The glass with water is cooled with a mixture of ice and salt. When the temperature reaches 1 ° with vigorous stirring, 106.75 g of p- (dimethylchlorosilyl) benzoic acid chloride are added with frequent drops. At the end of the acid chloride supply, the contents of the glass are stirred for 30 minutes, after which they are quickly transferred to a Büchner funnel to separate tetramethyldiphenyl disiloxanecarboxylic acid (4.4) acid crystals from the hydrochloric acid formed. The crystals on the filter are washed 3 times with water cooled to 1 °, squeezed, then immediately placed in a vacuum desiccator, where they are dried over sulfuric acid. Obtain 90 g of the acid chloride with t. PL. 54-55 ° and a chlorine content of 17.31%.

№ 152238- 2 Предмет изобретени No. 152238- 2 Subject of the invention

Способ получени  хлорангидрида симметричной тетраметилдифенилдисилоксапдикарбоновой- (4,4) кислоты, отличающийс  тем,, что, с целью расширени  сырьевой базы дл  получени  высокомолеку.л рных полимеров, хлорангидрид п-(диметилхлорсилил) бензойной кислоты гидролизуют водой при температуре не выше 1°.The method of obtaining the acid chloride with symmetric tetramethyldiphenyl disiloxapicarboxylic- (4,4) acid, characterized in that, in order to expand the raw material base to obtain high molecular weight polymers, p- (dimethylchlorosilyl) benzoic acid chloride is hydrolyzed with water at a temperature not higher than 2 °.

SU773746A 1962-04-12 1962-04-12 The method of obtaining the acid chloride symmetric tetramethyldiphenyldisiloxanecarboxy- (4,4 ') acid SU152238A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU773746A SU152238A1 (en) 1962-04-12 1962-04-12 The method of obtaining the acid chloride symmetric tetramethyldiphenyldisiloxanecarboxy- (4,4 ') acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU773746A SU152238A1 (en) 1962-04-12 1962-04-12 The method of obtaining the acid chloride symmetric tetramethyldiphenyldisiloxanecarboxy- (4,4 ') acid

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SU152238A1 true SU152238A1 (en) 1962-11-30

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3931552A (en) 1969-03-06 1976-01-06 P. R. Mallory & Co., Inc. Capacitor electrolyte
EP0394783A2 (en) * 1989-04-28 1990-10-31 General Electric Company Method for making carboxy aryl terminated organosiloxanes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3931552A (en) 1969-03-06 1976-01-06 P. R. Mallory & Co., Inc. Capacitor electrolyte
EP0394783A2 (en) * 1989-04-28 1990-10-31 General Electric Company Method for making carboxy aryl terminated organosiloxanes

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