Method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane
The invention discloses a method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane. The method comprises the following steps: in the presence of a high boiling point solvent N,N-diethyl formamide, heating to be 110-130 DEG C to enable diethylamine and 3-chloropropy trimethoxy silane to react...
Gespeichert in:
Hauptverfasser: | , , |
---|---|
Format: | Patent |
Sprache: | chi ; eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | Xi Yanan Che Hong Zhong Qijun |
description | The invention discloses a method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane. The method comprises the following steps: in the presence of a high boiling point solvent N,N-diethyl formamide, heating to be 110-130 DEG C to enable diethylamine and 3-chloropropy trimethoxy silane to react at normal pressure, performing refluxing reaction for 6-10 hours, cooling to be 20 DEG C, filtering off solid diethylamine hydrochloride, and leaching once by using the solvent N,N-diethyl formamide; performing vacuum concentration on the filtrate, recycling the solvent N,N-diethyl formamide, and rectifying so as to obtain a 99% product; dissolving the solid diethylamine hydrochloride in a solution, dripping into a sodium hydroxide solution, distilling so as to recycle diethylamine, absorbing the gas generated in the reaction and aftertreatment process by using the solvent N,N-diethyl formamide, and reusing in the production process. By adopting the method, not only is the reaction time great shortened, but also t |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN105837616A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN105837616A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN105837616A3</originalsourceid><addsrcrecordid>eNrjZHDwTS3JyE9RSMsvUigoSi1ILMrMS1fw0_HTTckEylTm6BrrJuZm5uUXFOUXVOYolBRl5oJ0VFQqFGfmJOal8jCwpiXmFKfyQmluBkU31xBnD93Ugvz41OKCxOTUvNSSeGc_QwNTC2NzM0MzR2Ni1AAAtbIxSQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane</title><source>esp@cenet</source><creator>Xi Yanan ; Che Hong ; Zhong Qijun</creator><creatorcontrib>Xi Yanan ; Che Hong ; Zhong Qijun</creatorcontrib><description>The invention discloses a method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane. The method comprises the following steps: in the presence of a high boiling point solvent N,N-diethyl formamide, heating to be 110-130 DEG C to enable diethylamine and 3-chloropropy trimethoxy silane to react at normal pressure, performing refluxing reaction for 6-10 hours, cooling to be 20 DEG C, filtering off solid diethylamine hydrochloride, and leaching once by using the solvent N,N-diethyl formamide; performing vacuum concentration on the filtrate, recycling the solvent N,N-diethyl formamide, and rectifying so as to obtain a 99% product; dissolving the solid diethylamine hydrochloride in a solution, dripping into a sodium hydroxide solution, distilling so as to recycle diethylamine, absorbing the gas generated in the reaction and aftertreatment process by using the solvent N,N-diethyl formamide, and reusing in the production process. By adopting the method, not only is the reaction time great shortened, but also t</description><language>chi ; eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2016</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20160810&DB=EPODOC&CC=CN&NR=105837616A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20160810&DB=EPODOC&CC=CN&NR=105837616A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Xi Yanan</creatorcontrib><creatorcontrib>Che Hong</creatorcontrib><creatorcontrib>Zhong Qijun</creatorcontrib><title>Method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane</title><description>The invention discloses a method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane. The method comprises the following steps: in the presence of a high boiling point solvent N,N-diethyl formamide, heating to be 110-130 DEG C to enable diethylamine and 3-chloropropy trimethoxy silane to react at normal pressure, performing refluxing reaction for 6-10 hours, cooling to be 20 DEG C, filtering off solid diethylamine hydrochloride, and leaching once by using the solvent N,N-diethyl formamide; performing vacuum concentration on the filtrate, recycling the solvent N,N-diethyl formamide, and rectifying so as to obtain a 99% product; dissolving the solid diethylamine hydrochloride in a solution, dripping into a sodium hydroxide solution, distilling so as to recycle diethylamine, absorbing the gas generated in the reaction and aftertreatment process by using the solvent N,N-diethyl formamide, and reusing in the production process. By adopting the method, not only is the reaction time great shortened, but also t</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2016</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZHDwTS3JyE9RSMsvUigoSi1ILMrMS1fw0_HTTckEylTm6BrrJuZm5uUXFOUXVOYolBRl5oJ0VFQqFGfmJOal8jCwpiXmFKfyQmluBkU31xBnD93Ugvz41OKCxOTUvNSSeGc_QwNTC2NzM0MzR2Ni1AAAtbIxSQ</recordid><startdate>20160810</startdate><enddate>20160810</enddate><creator>Xi Yanan</creator><creator>Che Hong</creator><creator>Zhong Qijun</creator><scope>EVB</scope></search><sort><creationdate>20160810</creationdate><title>Method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane</title><author>Xi Yanan ; Che Hong ; Zhong Qijun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN105837616A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2016</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>Xi Yanan</creatorcontrib><creatorcontrib>Che Hong</creatorcontrib><creatorcontrib>Zhong Qijun</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Xi Yanan</au><au>Che Hong</au><au>Zhong Qijun</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane</title><date>2016-08-10</date><risdate>2016</risdate><abstract>The invention discloses a method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane. The method comprises the following steps: in the presence of a high boiling point solvent N,N-diethyl formamide, heating to be 110-130 DEG C to enable diethylamine and 3-chloropropy trimethoxy silane to react at normal pressure, performing refluxing reaction for 6-10 hours, cooling to be 20 DEG C, filtering off solid diethylamine hydrochloride, and leaching once by using the solvent N,N-diethyl formamide; performing vacuum concentration on the filtrate, recycling the solvent N,N-diethyl formamide, and rectifying so as to obtain a 99% product; dissolving the solid diethylamine hydrochloride in a solution, dripping into a sodium hydroxide solution, distilling so as to recycle diethylamine, absorbing the gas generated in the reaction and aftertreatment process by using the solvent N,N-diethyl formamide, and reusing in the production process. By adopting the method, not only is the reaction time great shortened, but also t</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | chi ; eng |
recordid | cdi_epo_espacenet_CN105837616A |
source | esp@cenet |
subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | Method for preparing N,N-diethyl-3-aminopropyl trimethoxy silane |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T23%3A54%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=Xi%20Yanan&rft.date=2016-08-10&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN105837616A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |