SU138030A1 - The method of producing polycarbonates - Google Patents

The method of producing polycarbonates

Info

Publication number
SU138030A1
SU138030A1 SU668906A SU668906A SU138030A1 SU 138030 A1 SU138030 A1 SU 138030A1 SU 668906 A SU668906 A SU 668906A SU 668906 A SU668906 A SU 668906A SU 138030 A1 SU138030 A1 SU 138030A1
Authority
SU
USSR - Soviet Union
Prior art keywords
polycarbonates
producing polycarbonates
diphenylolpropane
producing
ester
Prior art date
Application number
SU668906A
Other languages
Russian (ru)
Inventor
И.Б. Бесфамильный
Т.Д. Кострюкова
В.Н. Котрелев
Original Assignee
И.Б. Бесфамильный
Т.Д. Кострюкова
В.Н. Котрелев
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 И.Б. Бесфамильный, Т.Д. Кострюкова, В.Н. Котрелев filed Critical И.Б. Бесфамильный
Priority to SU668906A priority Critical patent/SU138030A1/en
Application granted granted Critical
Publication of SU138030A1 publication Critical patent/SU138030A1/en

Links

Landscapes

  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Во всех известных способах получени  поликарбонатов чистота исходных продуктов  вл етс  важнейшим условием получени  полимеров с комплексом ценных свойств.In all known methods for producing polycarbonates, the purity of the starting products is the most important condition for obtaining polymers with a complex of valuable properties.

Особенно затруднено получение чистого 4,4-диоксидифенил-2,2-пропана ,  вл ющегос  основным сырьем дл  получени  поликарбонатов. Очистка этого продукта до нужной дл  синтеза поликарбонатов степени чистоты, т. е. до получени  вещества с температурой плавлени  156- 157°, требует неоднократной перекристаллизации его из уксусной кислоты или хлорбензола.The preparation of pure 4,4-dioxydiphenyl-2,2-propane, which is the main raw material for the production of polycarbonates, is particularly difficult. Purification of this product to the desired purity for the synthesis of polycarbonates, i.e., to obtain a substance with a melting point of 156-157 °, requires repeated recrystallization of it from acetic acid or chlorobenzene.

Предл.оженный новый способ получени  поликарбонатов конденсацией дифенилолпропана с метиловым эфиром хлоругольной кислоты в присутствии пиридина позвол ет использовать технический дифенилолпропан без его предварительной очистки, дл  чего процесс ведут в две стадии - с однократной перекристаллизацией образующегос  полупродукта из метилового спирта и переэтерификацией его в присутствии оксиметилата натри  и тетрабутоксититана.The proposed new method of producing polycarbonates by condensation of diphenylolpropane with chlorotic acid methyl ester in the presence of pyridine allows technical diphenylolpropane to be used without preliminary purification, for which the process is carried out in two stages — with a single recrystallization of the resulting intermediate from methyl alcohol and transesterification of it in the presence of hydroxymethyl in the presence of oximethyl and tetrabutoxytitanium.

Исходным продуктом дл  проведени  описанного синтеза служит технический дифенилолпропан с температурой плавлени  150-15Г.The starting product for carrying out the described synthesis is technical diphenylolpropane with a melting point of 150-15 °.

В первой стадии из дифенилолпропана и монометилового эфира хлоругольной кислоты в среде пиридина, который примен ют дл  св зывани  выдел ющегос  хлористого водорода, получают 4,4-диоксидикарбометоксидифенил-2 ,2-пропан (в дальнейщем называемый - эфир ДМ). Реакци  протекает по следующей схеме:In the first stage, 4,4-dioxydicarbomethoxydiphenyl-2, 2-propane (hereinafter referred to as DM ester) is obtained from diphenylolpropane and chlorogolic acid monomethyl ester in pyridine, which is used to bind the released hydrogen chloride. The reaction proceeds as follows:

СНзОСНзСНзSNSOSNzSNz

I/II / i

НО - СбН4-С-СеН4ОН f С О- СНзО-С-О - QH, - C-QH,-O1V 11BUT - SbN4-C-CeH4OH f C O-CH3-CO-O - QH, - C-QH, -O1V 11

СНзС1оСНзСНзС1оСНз

-С-ОСНз-ь2НС1-С-ОСНз-22НС1

SU668906A 1960-06-01 1960-06-01 The method of producing polycarbonates SU138030A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU668906A SU138030A1 (en) 1960-06-01 1960-06-01 The method of producing polycarbonates

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU668906A SU138030A1 (en) 1960-06-01 1960-06-01 The method of producing polycarbonates

Publications (1)

Publication Number Publication Date
SU138030A1 true SU138030A1 (en) 1960-11-30

Family

ID=48294204

Family Applications (1)

Application Number Title Priority Date Filing Date
SU668906A SU138030A1 (en) 1960-06-01 1960-06-01 The method of producing polycarbonates

Country Status (1)

Country Link
SU (1) SU138030A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3359242A (en) * 1963-08-19 1967-12-19 Huels Chemische Werke Ag Process for producing high molecular weight (cyclo) aliphatic polyesters of carbonicacid with (cyclo) glycols
US3506623A (en) * 1967-10-30 1970-04-14 Huels Chemische Werke Ag Process for producing high molecular weight (cyclo) aliphatic polyesters of carbonic acid with (cyclo) glycols

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3359242A (en) * 1963-08-19 1967-12-19 Huels Chemische Werke Ag Process for producing high molecular weight (cyclo) aliphatic polyesters of carbonicacid with (cyclo) glycols
US3506623A (en) * 1967-10-30 1970-04-14 Huels Chemische Werke Ag Process for producing high molecular weight (cyclo) aliphatic polyesters of carbonic acid with (cyclo) glycols

Similar Documents

Publication Publication Date Title
SU137511A1 (en) The method of obtaining complex alpha-alkenyl esters
SU421177A3 (en) METHOD OF OBTAINING LOWER ALKYL ETHER (±) DEN-CHRYZANTEMIC ACID
SU138030A1 (en) The method of producing polycarbonates
SU513622A3 (en) Method for preparing 4-hydroxymethyl-1,2-dihydro-1-phthalazone
US2533086A (en) Hydroxymethylthianaphthene
SU857104A1 (en) Method of producing saturated c4-c6 aldehydes
SU133887A1 (en) Method for isolating 2,5-lutidine
US2691039A (en) Stilbene-alpha-ketol compounds and process for making the same
SU455943A1 (en) Method for producing ethyl ester = nitrobenzoic acid
SU145244A1 (en) The method of obtaining esters of Kamenovo acid
SU397500A1 (en) FUND OF EXPERTS
US3390153A (en) Process for preparing 4-methyl-5-alkoxy oxazoles
SU659556A1 (en) Method of obtaining p-diiodo-benzene
US1304989A (en) Joseph koetschet abfb maurice betjdet
SU137926A1 (en) The method of obtaining 3, 8-dimethoxy- 4, 5, 6, 7-dibenzo-1, 2-dioxocyclooctane
SU467054A1 (en) The method of obtaining 1,4-dichlorobutane
US2946816A (en) Method of synthesis of dialkyl alphaketoglutarate from alkyl 2-furoate
SU218864A1 (en) The method of obtaining nitrate-3-nitrobutanol-2
US2982772A (en) Octahydro-5ah, 10ah, 4a, 9a-epoxydibenzo-p-dioxin-5a, 10a-diol
US3364222A (en) Process for preparing lower alkyl-2-ethylisonicotinic acid esters which are used as intermediates in the preparation of 2-ethylisonicotinic acid thiamide
DE854522C (en) Process for the production of degradation products of kakothelin or similarly constructed brucine derivatives
SU502896A1 (en) The method of obtaining bis (priortilsilyl) sulfates
SU147710A1 (en) The method of obtaining vanilla
SU483393A1 (en) Method for preparing adamantylacetic acids
SU134267A1 (en) The method of obtaining hypoxanthine (alpha-oxypurine)