Method of producing alkoxysioanes

专利摘要:
: The present invention relates to a process for the esterification of halosilanes by reaction with alcohols, characterized in that the reaction takes place in the presence of chlorohydrocarbons and in the absence of acid-binding means. The alcohols are selected from the group consisting of primary or secondary alcohols and phenols. Several organosilaneesters are used as building preservative agents. A number of other organosilaneesters and hydrogensilane esters have increasing technical importance for the synthesis of very valuable organofunctional silanes,
公开号:SU1233802A3
申请号:SU802979302
申请日:1980-09-10
公开日:1986-05-23
发明作者:Дитер Зайлер Клаус；Иоахим Валензик Ганс；Иоахим Кетцш Ганс
申请人:Динамит Нобель Аг (Фирма)；
IPC主号:

专利说明:

f
This invention relates to the chemistry of silicon-containing compounds, in particular to an improved process for the preparation of alkoxysilanes of the general formula
RraSi (OR),
where R is lower alkyl, unsubstituted or substituted by chlorine;
R is C, —C, alkyl or benzyl;
m - 1 or 2,
which can be used to make silicon varnishes, resins, etc.
The purpose of the invention is to increase the yield of the target product.
Example 1 In a heated three-necked flask with a capacity of 6 liters, equipped with a stirrer, reflux, with a pipe for removal of exhaust gas and a dropping funnel, 1060 g (5 mol) y-chloropropyltrichlorosilane and 900 ml of trichlorethylene are fed. After the mixture was heated to boiling with stirring, portions (20 ml) were added 930 g (15.5 mol of n-propanol). chloropropyl-tri (propo.hxi) silane with a bp, 101 C.
Example 2 Example 1 is repeated with the difference that the alcohol is added in portions of 40 ml over 135 minutes. At the same time, 1325 g (94% of theory) of y-chloropropyl-tri- (propoxy) -silane are obtained, with a boiling point of 0. 1 ° C.
Example 3 The example is repeated with the difference that 1060 g (5 mol) - chloropropyltrichlorosilane is subjected to esterification in 900 ml of carbon tetrachloride. After distillation of carbon tetrachloride, 1350 g (96% of theory) of y-chloropropyltripropoxysilyl are obtained with t. kip. 2,101 ° C.
12338022
Example 4. Example 1 is repeated with the difference that 1060 g (5 mol) - chloropropyltrichlorosilane in a medium of 5 2.7 l of trichlorethylene is esterified. After trichlorethylene was distilled off, 1370 g (97.2% of theory) of y-chloropropyltripropoxysilane were obtained with a bp. ,, 101 C.
P) e and measure 5. Repeat example, with the difference that 785 g (5 mol) of diethyldichlorosilane is subjected to esterification in 2 l of tetrachloroethylene. After distilling off tetrachloro ethylene, 971 g (95.2% of titanium soda) of diethyldipropoxysilane are obtained, b.p.
.
Example 6. Example 1 is repeated, with the difference that 745 g (5 mol) of methyl trichlorosilane is subjected to this test 1680 g (15.5 mol) of benzihydric alcohol in a medium of 1900 ml of tetrachlorethylene. After the distillation of tetrachloroethylene, 1750 g (96.5% of theory) of methyltribenyloxy-25 lan is obtained with a bp, 120 C.
Example 7. The example is repeated with the difference that 1060 g (5 mol) -chloropropyltrichlorosilane is subjected to esterification 906 g
30 (15.5 mol) of isopropanol in the environment
1900 ml of trichlorethylene. After trichlorethylene distillation, 98 g (96.2% of theory) of jC-chloroprogyltriisopropoxysilane are obtained with a bp. 107 s,
3 Example 8. Example I is repeated with the difference that the esterification reaction is carried out in a medium of 3 liters of I, 2-dichloroethane. After distillation of 1,2-dichloroethane, 1360 g are obtained (96.8%
40 theory) of a product that is identical with the product of example I.
Thus, the proposed method allows to obtain the desired product with a high ammoment.
Compiled by V. M kush: eva Editor M. Blanar Tehred, I. Popovrech Proofreader S. Cherni
Order 2787/59 Circulation: 343 The General Committee of the USSR
for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab., 4/5
Production and printing company,. Uzhgorod, st. Project, 4
RI) diethyldipropoxysilane with so Kip.
.
Example 6. Example 1 is repeated, with the difference that 745 g (5 mol) of methyl trichlorosilane is subjected to this test of 1680 g (15.5 mol) of benzic acid in 1900 ml of tetrachlorethylene. After distilling off tetrachloroethylene, 1750 g (96.5% of theory) of methyltribenyloxy silane are obtained, with a boiling point of 120 C.
Example 7. The example is repeated with the difference that 1060 g (5 mol) -chloropropyltrichlorosilane is subjected to esterification 906 g
(15.5 mol) of isopropanol in the environment
1900 ml of trichlorethylene. After trichlorethylene distillation, 98 g (96.2% of theory) of jC-chloroprogyltriisopropoxysilane are obtained with a bp. 107 s,
Example 8. Example I is repeated, with the difference that the esterification reaction is carried out in a medium of 3 liters of I, 2-dichloroethane. After distillation of 1,2-dichloroethane, 1360 g are obtained (96.8%
theory) of a product that is identical with the product of example I.
Thus, the proposed method allows to obtain the desired product with a high ammoment.

权利要求:
Claims (1)
[1]
METHOD FOR PRODUCING ALCOXIS-
LANOV of the general formula
RmSi (OR ¹ ), 'where R is lower alkyl, unsubstituted or substituted with chlorine;
R ¹ - C _f tC alkyl or benzyl; m is 1 or 2, by esterification of chlorosilane of the general formula where R and m have the indicated meanings, with an alcohol of the general formula r'ch, where R 'has the indicated meanings, at elevated temperature with the removal of the resulting hydrogen chloride, characterized in that, for the purpose of increasing the yield of the target product, the esterification is carried out in the presence of chlorinated methane, ethane or ethylene at the boiling point of the reaction mixture, while the alcohol is added in portions over 135-270 minutes.
SU "" 1233802 AZ

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引用文献:

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RU2565675C1|2014-05-30|2015-10-20|Федеральное государственное бюджетное учреждение науки Институт синтетических полимерных материалов им. Ениколопова Российской Академии Наук |Method of producing methylbenzyl alkoxysilanes|US2701803A|1948-10-20|1955-02-08|Socony Vacuum Oil Co Inc|Synthetic lubricants|

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BE814011A|1971-11-03|1974-08-16|Organosilanes prepn. from halo- or aminosilanes - by reaction with hydroxy or carboxy cpds. in pentane|

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DE2409731C2|1974-03-01|1983-05-26|Dynamit Nobel Ag, 5210 Troisdorf|Process for the esterification of trichlorosilane|DE2800017C2|1978-01-02|1983-05-26|Dynamit Nobel Ag, 5210 Troisdorf|Process for the preparation of organoalkoxysilanes|

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US4172805A|1978-02-27|1979-10-30|Dow Corning Corporation|Benzyloxy endblocked organosilicon dielectric fluids and electrical devices containing same|

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JPH0434875B2|1982-12-08|1992-06-09|Kitanippon Onkyo Kk|

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DE19755597A1|1997-12-15|1999-06-17|Huels Chemische Werke Ag|Process for the preparation of alkoxysilanes|

法律状态:

优先权:

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申请号 | 申请日 | 专利标题

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DE2532887A|DE2532887C2|1975-07-23|1975-07-23|Process for the esterification of halosilanes|

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