2,2,5,5,-Tetramethyl-2,5-disila-1,3-dioxolan und Verfahren zu seiner Herstellung
2,2,5,5 - Tetramethyl - 2,5 - disila - 1,3 - dioxolan of the formula may be prepared by two methods. One method comprises heating a mixture of equimolar amounts of 1,3 - di - (hydroxymethyl) - tetramethyldisiloxane and 1,3 - di(bromomethyl)-tetramethyl disiloxane and excess methylamine until salt p...
Gespeichert in:
Hauptverfasser: | , , |
---|---|
Format: | Patent |
Sprache: | ger |
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 | HANS SATTLEGGER,DR WALTER SIMMLER,DR HANS NIEDERPRUEM,DR |
description | 2,2,5,5 - Tetramethyl - 2,5 - disila - 1,3 - dioxolan of the formula may be prepared by two methods. One method comprises heating a mixture of equimolar amounts of 1,3 - di - (hydroxymethyl) - tetramethyldisiloxane and 1,3 - di(bromomethyl)-tetramethyl disiloxane and excess methylamine until salt precipitation is complete, removing the nitrogen compounds from the mixture, adding p-toluene sulphonic acid as catalyst, distilling under reduced pressure and recovering the product as the distilate. The second method comprises heating a mixture of equimolar amounts of dimethyl - (acetoxymethyl)-acetoxysilane and dimethyldiethoxysilane, 5-20 fold molar amount of methanol and p-toluene sulphonic acid as catalyst, distilling off methanol, ethanol and methyl acetate, and then distilling under reduced pressure and recovering the product as the distillate. Hydrolysis of the product alone gives 1,7-di-(hydroxymethyl)-octamethyltetrasiloxane and cohydrolysis with organoalkoxysilanes gives organopolysiloxanes with terminal hydroxymethyl groups. Copolymerization with trioxan gives polyoxymethylenes with siloxane segments. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_DE1493733A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>DE1493733A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_DE1493733A13</originalsourceid><addsrcrecordid>eNrjZAgw0jHSMQVC3ZDUkqLE3NSSjMocXaCQbkpmcWZOoq6hjjGQmV-Rn5OYp1Cal6IQllqUlphRlJqnUFWqUJyamZdapOCRWlRckpqTU5qXzsPAmpaYU5zKC6W5GRTcXEOcPXRTC_LjU4sLEpNT81JL4l1cDU0sjc2NjR0NjYlQAgCO4zQ2</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>2,2,5,5,-Tetramethyl-2,5-disila-1,3-dioxolan und Verfahren zu seiner Herstellung</title><source>esp@cenet</source><creator>HANS SATTLEGGER,DR ; WALTER SIMMLER,DR ; HANS NIEDERPRUEM,DR</creator><creatorcontrib>HANS SATTLEGGER,DR ; WALTER SIMMLER,DR ; HANS NIEDERPRUEM,DR</creatorcontrib><description>2,2,5,5 - Tetramethyl - 2,5 - disila - 1,3 - dioxolan of the formula <FORM:1080397/C3/1> may be prepared by two methods. One method comprises heating a mixture of equimolar amounts of 1,3 - di - (hydroxymethyl) - tetramethyldisiloxane and 1,3 - di(bromomethyl)-tetramethyl disiloxane and excess methylamine until salt precipitation is complete, removing the nitrogen compounds from the mixture, adding p-toluene sulphonic acid as catalyst, distilling under reduced pressure and recovering the product as the distilate. The second method comprises heating a mixture of equimolar amounts of dimethyl - (acetoxymethyl)-acetoxysilane and dimethyldiethoxysilane, 5-20 fold molar amount of methanol and p-toluene sulphonic acid as catalyst, distilling off methanol, ethanol and methyl acetate, and then distilling under reduced pressure and recovering the product as the distillate. Hydrolysis of the product alone gives 1,7-di-(hydroxymethyl)-octamethyltetrasiloxane and cohydrolysis with organoalkoxysilanes gives organopolysiloxanes with terminal hydroxymethyl groups. Copolymerization with trioxan gives polyoxymethylenes with siloxane segments.</description><language>ger</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>1969</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=19691120&DB=EPODOC&CC=DE&NR=1493733A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19691120&DB=EPODOC&CC=DE&NR=1493733A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>HANS SATTLEGGER,DR</creatorcontrib><creatorcontrib>WALTER SIMMLER,DR</creatorcontrib><creatorcontrib>HANS NIEDERPRUEM,DR</creatorcontrib><title>2,2,5,5,-Tetramethyl-2,5-disila-1,3-dioxolan und Verfahren zu seiner Herstellung</title><description>2,2,5,5 - Tetramethyl - 2,5 - disila - 1,3 - dioxolan of the formula <FORM:1080397/C3/1> may be prepared by two methods. One method comprises heating a mixture of equimolar amounts of 1,3 - di - (hydroxymethyl) - tetramethyldisiloxane and 1,3 - di(bromomethyl)-tetramethyl disiloxane and excess methylamine until salt precipitation is complete, removing the nitrogen compounds from the mixture, adding p-toluene sulphonic acid as catalyst, distilling under reduced pressure and recovering the product as the distilate. The second method comprises heating a mixture of equimolar amounts of dimethyl - (acetoxymethyl)-acetoxysilane and dimethyldiethoxysilane, 5-20 fold molar amount of methanol and p-toluene sulphonic acid as catalyst, distilling off methanol, ethanol and methyl acetate, and then distilling under reduced pressure and recovering the product as the distillate. Hydrolysis of the product alone gives 1,7-di-(hydroxymethyl)-octamethyltetrasiloxane and cohydrolysis with organoalkoxysilanes gives organopolysiloxanes with terminal hydroxymethyl groups. Copolymerization with trioxan gives polyoxymethylenes with siloxane segments.</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>1969</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZAgw0jHSMQVC3ZDUkqLE3NSSjMocXaCQbkpmcWZOoq6hjjGQmV-Rn5OYp1Cal6IQllqUlphRlJqnUFWqUJyamZdapOCRWlRckpqTU5qXzsPAmpaYU5zKC6W5GRTcXEOcPXRTC_LjU4sLEpNT81JL4l1cDU0sjc2NjR0NjYlQAgCO4zQ2</recordid><startdate>19691120</startdate><enddate>19691120</enddate><creator>HANS SATTLEGGER,DR</creator><creator>WALTER SIMMLER,DR</creator><creator>HANS NIEDERPRUEM,DR</creator><scope>EVB</scope></search><sort><creationdate>19691120</creationdate><title>2,2,5,5,-Tetramethyl-2,5-disila-1,3-dioxolan und Verfahren zu seiner Herstellung</title><author>HANS SATTLEGGER,DR ; WALTER SIMMLER,DR ; HANS NIEDERPRUEM,DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE1493733A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1969</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>HANS SATTLEGGER,DR</creatorcontrib><creatorcontrib>WALTER SIMMLER,DR</creatorcontrib><creatorcontrib>HANS NIEDERPRUEM,DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HANS SATTLEGGER,DR</au><au>WALTER SIMMLER,DR</au><au>HANS NIEDERPRUEM,DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>2,2,5,5,-Tetramethyl-2,5-disila-1,3-dioxolan und Verfahren zu seiner Herstellung</title><date>1969-11-20</date><risdate>1969</risdate><abstract>2,2,5,5 - Tetramethyl - 2,5 - disila - 1,3 - dioxolan of the formula <FORM:1080397/C3/1> may be prepared by two methods. One method comprises heating a mixture of equimolar amounts of 1,3 - di - (hydroxymethyl) - tetramethyldisiloxane and 1,3 - di(bromomethyl)-tetramethyl disiloxane and excess methylamine until salt precipitation is complete, removing the nitrogen compounds from the mixture, adding p-toluene sulphonic acid as catalyst, distilling under reduced pressure and recovering the product as the distilate. The second method comprises heating a mixture of equimolar amounts of dimethyl - (acetoxymethyl)-acetoxysilane and dimethyldiethoxysilane, 5-20 fold molar amount of methanol and p-toluene sulphonic acid as catalyst, distilling off methanol, ethanol and methyl acetate, and then distilling under reduced pressure and recovering the product as the distillate. Hydrolysis of the product alone gives 1,7-di-(hydroxymethyl)-octamethyltetrasiloxane and cohydrolysis with organoalkoxysilanes gives organopolysiloxanes with terminal hydroxymethyl groups. Copolymerization with trioxan gives polyoxymethylenes with siloxane segments.</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | ger |
recordid | cdi_epo_espacenet_DE1493733A1 |
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 | 2,2,5,5,-Tetramethyl-2,5-disila-1,3-dioxolan und Verfahren zu seiner Herstellung |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T16%3A42%3A35IST&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=HANS%20SATTLEGGER,DR&rft.date=1969-11-20&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EDE1493733A1%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 |