Preparation method for isoalkylalkenyloxysilane

A technology of isoalkenyloxysilane and chlorosilane, which is applied in the field of preparation of isoalkenyloxysilane, can solve the problems of unfavorable industrial production application, low operation safety, high temperature and high pressure, etc., and achieve the advantages of industrial production, The effect of high safety and reduction of production cost

Inactive Publication Date: 2018-04-20
湖北新蓝天新材料股份有限公司
View PDF1 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there are few reports on the synthesis of isoalkenyloxysilanes. Usually, cuprous chloride is used as a catalyst, triethylamine is used as an acid-binding agent, and toxic aromatic compounds are used as solvents. The reaction time is as long as 20 to 50 hours. Reaction of alkyltrichlorosilane and alkyl ketone to produce alkylisoalkenyloxysilane silane yield less than 50%
Among them, there are literature reports that the yield of vinyl triisopropenyloxysilane is 45.7%, and related literature reports that the yield of phenyl triisopropenoxysilane is 43%. The isoalkenyloxysilane prepared by the above method In addition to the low yield, there are also the following disadvantages: the use of toxic benzene compounds as solvents, low operational safety, long reaction time, high cost, and high temperature and high pressure are required, which is not conducive to industrial production and application

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0024] The embodiment of the present invention provides a preparation method of isoalkenyloxysilane, which comprises the following steps:

[0025] S1: put alkyl ketone, acid-binding agent and catalyst into the reaction kettle, the mass ratio of alkyl ketone, acid-binding agent and catalyst is 1000:1090:1-5, and heat to the temperature of the kettle while stirring to 40°C;

[0026] S2: Keep the temperature of the kettle at 20°C-60°C, add chlorosilane dropwise to the reactor for 20min-40min, and then keep warm and reflux after the addition of chlorosilane until the content of isoalkeneoxysilane in the reactor is greater than 30 %, airtightly filter the tertiary amine hydrochloride solid to obtain the first filtrate; distill the first filtrate under normal pressure, reclaim the unreacted alkyl ketone and acid-binding agent, and obtain the first mother liquor;

[0027] S3: Add solid paraffin and chloride ion neutralizer to the first mother liquor, keep the temperature of the kettl...

Embodiment 1

[0041] This embodiment provides a kind of preparation method of isoalkenyloxysilane, which comprises the following steps:

[0042] S1: Put 224g of acetone, 224g of triethylamine and 0.224g of cuprous chloride into the reaction kettle at one time, and heat it until the temperature of the kettle is 40°C while stirring;

[0043] S2: Keep the temperature of the kettle at 20°C to 60°C, add 100g of vinyltrichlorosilane dropwise to the reactor, and finish dropping in 20min to 25min. The reaction time is 48h, until the vinyltriisopropenyloxysilane content in the reactor is greater than 30%, airtightly filter the tertiary amine hydrochloride solid to obtain the first filtrate; distill the first filtrate under normal pressure, recover unreacted acetone and Triethylamine, obtains the first mother liquor;

[0044] S3: Add 28.4g of crude paraffin and 5.68g of zinc stearate to the first mother liquor, keep the temperature of the kettle at 40°C-60°C, and the reaction time is 2h, and then fi...

Embodiment 2

[0048] This embodiment provides a kind of preparation method of isoalkenyloxysilane, which comprises the following steps:

[0049] S1: Put 224g of acetone, 244g of tripropylamine and 0.45g of stannous chloride into the reaction kettle at one time, and heat it until the temperature of the kettle is 40°C while stirring;

[0050] S2: Keep the temperature of the kettle at 20°C to 60°C, add 150g of vinyltrichlorosilane dropwise to the reactor, and finish dropping in 30min to 40min. The reaction time is 48h, until the vinyltriisopropenyloxysilane content in the reactor is greater than 30%, airtightly filter the tertiary amine hydrochloride solid to obtain the first filtrate; distill the first filtrate under normal pressure, recover unreacted acetone and Tripropylamine obtains the first mother liquor;

[0051] S3: Add 30.9g of semi-refined paraffin and 61.8g of zinc stearate to the first mother liquor, keep the temperature of the kettle at 40°C-60°C, the reaction time is 1h, and the...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a preparation method for isoalkylalkenyloxysilane. The preparation method comprises the following steps: adding alkyl ketone, an acid binding agent and a catalyst in a mass ratio of 1000: 1090: (1-5) into a reaction vessel, and carrying out heating under stirring until the temperature of the reaction vessel is 40 DEG C; maintaining the temperature of the reaction vessel tobe 20 to 60 DEG C, adding chlorosilane into the reaction vessel drop by drop within 20 to 40 min, carrying out heat-preserved reflux after completion of addition of chlorosilane until the content of isoalkylalkenyloxysilane in the reaction vessel is greater than 30%, and hermetically filtering out a tertiary amine hydrochloride solid so as to obtain a first filtrate; subjecting the first filtrateto distillation at normal pressure so as to first mother liquor; adding solid paraffin and a chloride ion neutralizer into the first mother liquor, maintaining the temperature of the reaction vessel to be 40 to 60 DEG C, carrying out a reaction for 1 to 3 h, and then carrying out filtering under the condition that vessel temperature is 35 to 40 DEG C so as to obtain a second filtrate; and subjecting the second filtrate to vacuum rectification at a temperature of 124 to 126 DEG C and a pressure of 0.0130 to 0.0140 MPa so as to obtain isoalkylalkenyloxysilane. The isoalkylalkenyloxysilane prepared in the invention has a purity of 94% or above and yield of more than 63%.

Description

technical field [0001] The invention relates to a preparation method of isoalkenyloxysilane, in particular to a method for preparing isoalkenyloxysilane by the isomerization method of alkyl ketone. Background technique [0002] Isoalkenyloxysilane is a kind of silane crosslinking agent with special application. Because the molecular structure contains isoalkenyloxy group and functional group of alkyl, alkenyl or phenyl, it is widely used in the treatment of polyethylene, polypropylene, Unsaturated polyester and other polymers are modified to give them excellent pressure cracking resistance, memory, wear resistance and impact resistance; to improve the affinity between glass fibers, inorganic fillers and vinyl-reactive resins, It is often used for the aging resistance of silane cross-linked polyethylene cables and pipes; it can be copolymerized with acrylic paints to make special exterior wall coatings, which have good weather resistance and dust resistance; it is used for cr...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07F7/18C07F7/20
CPCC07F7/1804C07F7/188C07F7/20
Inventor 冯琼华肖俊平王成
Owner 湖北新蓝天新材料股份有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products