VERFAHREN ZUR HERSTELLUNG VON CARBONYLFLUORID

Process for the preparation of aliphatic fluoroformates by reaction of carbonyl fluoride with an aliphatic alcohol in the presence of sodium fluoride in an ether solvent at -20 to +50 degrees C is new. The sodium fluoride is preferably a powder with a specific surface area of 0.1 m2/ g or more and a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: GRENOUILLAT, DENIS, DELABROUILLE, PHILIPPE, SENET, JEAN-PIERRE, SENNYEY, GERARD
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 GRENOUILLAT, DENIS
DELABROUILLE, PHILIPPE
SENET, JEAN-PIERRE
SENNYEY, GERARD
description Process for the preparation of aliphatic fluoroformates by reaction of carbonyl fluoride with an aliphatic alcohol in the presence of sodium fluoride in an ether solvent at -20 to +50 degrees C is new. The sodium fluoride is preferably a powder with a specific surface area of 0.1 m2/ g or more and a particle size below 20 mum. Preferably 1.1 to 2 moles of carbonyl fluoride are used per mole of alcohol, suitable solvents being tert. butyl methyl ether, dioxan, tetrahydrofuran, 2-methyl tetrahydrofuran, dibenzyl ether, and ethylene glycol or polyethylene glycol dimethyl ethers. The carbonyl fluoride is prepared by reaction of phosgene, diphosgene, or triphosgene or their mixtures with excess powdered sodium fluoride in a polar aprotic solvent such as acetonitrile, at 25 - 120 degrees C, followed by condensation of the resultant gas at 0 to -50 degrees C.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_DE60008710TT2</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>DE60008710TT2</sourcerecordid><originalsourceid>FETCH-epo_espacenet_DE60008710TT23</originalsourceid><addsrcrecordid>eNrjZNANcw1yc_QIcvVTiAoNUvBwDQoOcfXxCfVzVwjz91Nwdgxy8veL9HHzCfUP8nThYWBNS8wpTuWF0twMSm6uIc4euqkF-fGpxQWJyal5qSXxLq5mBgYGFuaGBiEhRsZEKQIAPF0mlQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>VERFAHREN ZUR HERSTELLUNG VON CARBONYLFLUORID</title><source>esp@cenet</source><creator>GRENOUILLAT, DENIS ; DELABROUILLE, PHILIPPE ; SENET, JEAN-PIERRE ; SENNYEY, GERARD</creator><creatorcontrib>GRENOUILLAT, DENIS ; DELABROUILLE, PHILIPPE ; SENET, JEAN-PIERRE ; SENNYEY, GERARD</creatorcontrib><description>Process for the preparation of aliphatic fluoroformates by reaction of carbonyl fluoride with an aliphatic alcohol in the presence of sodium fluoride in an ether solvent at -20 to +50 degrees C is new. The sodium fluoride is preferably a powder with a specific surface area of 0.1 m2/ g or more and a particle size below 20 mum. Preferably 1.1 to 2 moles of carbonyl fluoride are used per mole of alcohol, suitable solvents being tert. butyl methyl ether, dioxan, tetrahydrofuran, 2-methyl tetrahydrofuran, dibenzyl ether, and ethylene glycol or polyethylene glycol dimethyl ethers. The carbonyl fluoride is prepared by reaction of phosgene, diphosgene, or triphosgene or their mixtures with excess powdered sodium fluoride in a polar aprotic solvent such as acetonitrile, at 25 - 120 degrees C, followed by condensation of the resultant gas at 0 to -50 degrees C.</description><edition>7</edition><language>ger</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2005</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&amp;date=20050210&amp;DB=EPODOC&amp;CC=DE&amp;NR=60008710T2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20050210&amp;DB=EPODOC&amp;CC=DE&amp;NR=60008710T2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>GRENOUILLAT, DENIS</creatorcontrib><creatorcontrib>DELABROUILLE, PHILIPPE</creatorcontrib><creatorcontrib>SENET, JEAN-PIERRE</creatorcontrib><creatorcontrib>SENNYEY, GERARD</creatorcontrib><title>VERFAHREN ZUR HERSTELLUNG VON CARBONYLFLUORID</title><description>Process for the preparation of aliphatic fluoroformates by reaction of carbonyl fluoride with an aliphatic alcohol in the presence of sodium fluoride in an ether solvent at -20 to +50 degrees C is new. The sodium fluoride is preferably a powder with a specific surface area of 0.1 m2/ g or more and a particle size below 20 mum. Preferably 1.1 to 2 moles of carbonyl fluoride are used per mole of alcohol, suitable solvents being tert. butyl methyl ether, dioxan, tetrahydrofuran, 2-methyl tetrahydrofuran, dibenzyl ether, and ethylene glycol or polyethylene glycol dimethyl ethers. The carbonyl fluoride is prepared by reaction of phosgene, diphosgene, or triphosgene or their mixtures with excess powdered sodium fluoride in a polar aprotic solvent such as acetonitrile, at 25 - 120 degrees C, followed by condensation of the resultant gas at 0 to -50 degrees C.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2005</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNANcw1yc_QIcvVTiAoNUvBwDQoOcfXxCfVzVwjz91Nwdgxy8veL9HHzCfUP8nThYWBNS8wpTuWF0twMSm6uIc4euqkF-fGpxQWJyal5qSXxLq5mBgYGFuaGBiEhRsZEKQIAPF0mlQ</recordid><startdate>20050210</startdate><enddate>20050210</enddate><creator>GRENOUILLAT, DENIS</creator><creator>DELABROUILLE, PHILIPPE</creator><creator>SENET, JEAN-PIERRE</creator><creator>SENNYEY, GERARD</creator><scope>EVB</scope></search><sort><creationdate>20050210</creationdate><title>VERFAHREN ZUR HERSTELLUNG VON CARBONYLFLUORID</title><author>GRENOUILLAT, DENIS ; DELABROUILLE, PHILIPPE ; SENET, JEAN-PIERRE ; SENNYEY, GERARD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE60008710TT23</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>2005</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>GRENOUILLAT, DENIS</creatorcontrib><creatorcontrib>DELABROUILLE, PHILIPPE</creatorcontrib><creatorcontrib>SENET, JEAN-PIERRE</creatorcontrib><creatorcontrib>SENNYEY, GERARD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>GRENOUILLAT, DENIS</au><au>DELABROUILLE, PHILIPPE</au><au>SENET, JEAN-PIERRE</au><au>SENNYEY, GERARD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>VERFAHREN ZUR HERSTELLUNG VON CARBONYLFLUORID</title><date>2005-02-10</date><risdate>2005</risdate><abstract>Process for the preparation of aliphatic fluoroformates by reaction of carbonyl fluoride with an aliphatic alcohol in the presence of sodium fluoride in an ether solvent at -20 to +50 degrees C is new. The sodium fluoride is preferably a powder with a specific surface area of 0.1 m2/ g or more and a particle size below 20 mum. Preferably 1.1 to 2 moles of carbonyl fluoride are used per mole of alcohol, suitable solvents being tert. butyl methyl ether, dioxan, tetrahydrofuran, 2-methyl tetrahydrofuran, dibenzyl ether, and ethylene glycol or polyethylene glycol dimethyl ethers. The carbonyl fluoride is prepared by reaction of phosgene, diphosgene, or triphosgene or their mixtures with excess powdered sodium fluoride in a polar aprotic solvent such as acetonitrile, at 25 - 120 degrees C, followed by condensation of the resultant gas at 0 to -50 degrees C.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language ger
recordid cdi_epo_espacenet_DE60008710TT2
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
title VERFAHREN ZUR HERSTELLUNG VON CARBONYLFLUORID
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T05%3A10%3A25IST&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=GRENOUILLAT,%20DENIS&rft.date=2005-02-10&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EDE60008710TT2%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