SU368276A1 - METHOD FOR OBTAINING TRIALCOXYLILYLKYL ZHIROVA OF THIO ACIDS OF THREE-VALENT MUSCLE - Google Patents

METHOD FOR OBTAINING TRIALCOXYLILYLKYL ZHIROVA OF THIO ACIDS OF THREE-VALENT MUSCLE

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Publication number
SU368276A1
SU368276A1 SU1634016A SU1634016A SU368276A1 SU 368276 A1 SU368276 A1 SU 368276A1 SU 1634016 A SU1634016 A SU 1634016A SU 1634016 A SU1634016 A SU 1634016A SU 368276 A1 SU368276 A1 SU 368276A1
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SU
USSR - Soviet Union
Prior art keywords
zhirova
trialcoxylilylkyl
valent
muscle
obtaining
Prior art date
Application number
SU1634016A
Other languages
Russian (ru)
Inventor
К. А. Мамаков Г. Камай витель Н. А. Чадаева
Original Assignee
Ордена Трудового Красного Знамени институт органической , физической химии А. Е. Арбузова
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Application filed by Ордена Трудового Красного Знамени институт органической , физической химии А. Е. Арбузова filed Critical Ордена Трудового Красного Знамени институт органической , физической химии А. Е. Арбузова
Priority to SU1634016A priority Critical patent/SU368276A1/en
Application granted granted Critical
Publication of SU368276A1 publication Critical patent/SU368276A1/en

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Изобретение относитс  к получению не описанных в литературе кремнийорганических производных ТИОКИСЛОТ трехвалентного мышь ка , которые обладают фунгицидной активностью и примен ютс  дл  изготовлени  покрытий , защищающих оптические детали от микробиологического обрастани .The invention relates to the production of organosilicon derivatives of trivalent arsenic acid Tioxyacid, which are not described in literature, which possess fungicidal activity and are used to make coatings that protect optical components from microbiological fouling.

Предлагаемый способ основан на реакции переэтерификации и заключаетс  во взаимодействии алкиловых эфиров кислот трехвалентного мыщь ка с триалкоксисилилалкилмеркаптанами при нагревании, например до кипени , с последующим выделением целевого продукта известными методами. Реакци  идет по схеме:The proposed method is based on the transesterification reaction and consists in the interaction of alkyl esters of trivalent mice with trialkoxysilylalkyl mercaptans when heated, for example until boiling, followed by isolation of the target product by known methods. The reaction goes according to the following scheme:

RJ, А8(ОЛ1К;з-п (3-п)НЗ()гпй1(ОК )з 5(CH.7)mSi(OR) (3-n)ALkOHRJ, A8 (OL1K; sn (3-p) NS) () gpy1 (OK) s 5 (CH.7) mSi (OR) (3-n) ALkOH

где R - алкил, арил, гетероцикл;where R is alkyl, aryl, heterocycle;

R - СНз или CsHs; Alk-СНзИли С2Н5; п -О, 1, 2; m -2, 3.R is CH3 or CsHs; Alk-CH3 or C2H5; n, 1, 2; m -2, 3.

Полученные тиоэфиры представл ют собой бесцветные или слабо окращенные в желтый цвет густые жидкости, обладающие слабым специфическим запахом. Они хорошо раствор ютс  в органических растворител х, гидролизуютс  водой с разрывом св зи кремний - кислород. Выход продуктов практически количественный . Продукты реакции не требуют очистки.The resulting thioethers are colorless or slightly yellow-colored thick liquids with a low specific odor. They dissolve well in organic solvents, hydrolyze with water to break the bond between silicon and oxygen. The yield of products is almost quantitative. The reaction products do not require purification.

Пример. Получение ди-р- (триэтоксисилил )-этилового эфира этилдитиоарсонистой кислоты.Example. Preparation of di-p- (triethoxysilyl) ethyl ethyl dithioaronic acid ester.

К 4,0 г диэтилового эфира этиларсонистой кислоты прибавл ют при перемещивании 9,25 г р-(триэтоксисилил)-этилмеркаптана, наблюда  небольшой разогрев смеси. Смесь нагревают до кипени , отгон ют образовавшийс  этанол, нагревают остаток на вод ной бане в вакууме дл  полного удалени  этанола и затем анализируют. Выход 11,3 г (99,9%).9.25 g of p- (triethoxysilyl) -ethyl mercaptan was added to 4.0 g of ethyl ethyl acetate diethyl, while slight mixing of the mixture was observed. The mixture is heated to boiling, the ethanol formed is distilled off, the residue is heated on a water bath under vacuum to completely remove the ethanol and then analyzed. The yield of 11.3 g (99.9%).

Найдено, %: As 13,05; 13,00; S 11,76; 11,60. Ci8H43AsS2Si2O6.Found,%: As 13.05; 13.00; S 11.76; 11.60. Ci8H43AsS2Si2O6.

Вычислено, %: As 13,60; S 11,64. Аналогично синтезируют соединени , перечислепные в таблице. Предмет изобретени  Способ получени  триалкоксисилилалкиловых эфиров тиокислот трехвалентного мышь ка , отличающийс  тем, что триалкоксисилил- 5 Густой мазеобразный продукт гр зно-зеленого цвета, не кристаллизующийс  при хранении. алкилмеркаптан обрабатывают алкиловым эфиром кислоты трехвалентного мышь ка при нагревании, например до кипени , с последуюш ,им выделением целевого продукта известными приемами.Calculated,%: As 13.60; S 11.64. Compounds listed in the table are synthesized in a similar way. The subject of the invention is a method for the preparation of trialkoxy-silylalkyl esters of trivalent arsenic thioacids, characterized in that trialkoxy-silyl-5 Dense greasy-green greasy-green product that does not crystallize during storage. The alkyl mercaptan is treated with the alkyl ester of the trivalent arsenic when heated, for example until boiling, followed by extracting the target product by known methods.

SU1634016A 1971-03-22 1971-03-22 METHOD FOR OBTAINING TRIALCOXYLILYLKYL ZHIROVA OF THIO ACIDS OF THREE-VALENT MUSCLE SU368276A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1634016A SU368276A1 (en) 1971-03-22 1971-03-22 METHOD FOR OBTAINING TRIALCOXYLILYLKYL ZHIROVA OF THIO ACIDS OF THREE-VALENT MUSCLE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1634016A SU368276A1 (en) 1971-03-22 1971-03-22 METHOD FOR OBTAINING TRIALCOXYLILYLKYL ZHIROVA OF THIO ACIDS OF THREE-VALENT MUSCLE

Publications (1)

Publication Number Publication Date
SU368276A1 true SU368276A1 (en) 1973-01-26

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Application Number Title Priority Date Filing Date
SU1634016A SU368276A1 (en) 1971-03-22 1971-03-22 METHOD FOR OBTAINING TRIALCOXYLILYLKYL ZHIROVA OF THIO ACIDS OF THREE-VALENT MUSCLE

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SU (1) SU368276A1 (en)

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