Improvements relating to Alkyl Phosphites

1,173,763. Alkyl phosphite derivatives. PURE CHEMICALS Ltd. 1 Aug., 1967 [8 Sept., 1966], No. 40116/66. Heading C2C. [Also in Division C3] A process for preparing alkyl phosphite derivatives comprises transesterifying a phosphite of formula (R2O) 3 P, where R2 is alkyl or aryl by liberation of the c...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: DAVID FREDERIC WATSON CROSS, VINCENT OAKES
Format: Patent
Sprache: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 DAVID FREDERIC WATSON CROSS
VINCENT OAKES
description 1,173,763. Alkyl phosphite derivatives. PURE CHEMICALS Ltd. 1 Aug., 1967 [8 Sept., 1966], No. 40116/66. Heading C2C. [Also in Division C3] A process for preparing alkyl phosphite derivatives comprises transesterifying a phosphite of formula (R2O) 3 P, where R2 is alkyl or aryl by liberation of the corresponding alcohol or phenol by reaction with at least two alcohols from the group consisting of alkanols, alkanediols, polyalkylene glycols, and hydrogenated bisphenols, one but not more than one being an alkanol, in the presence of an alkaline or secondary phosphite catalyst, the alcohol being present in such proportions as to enable three moles of alcohol or phenol to be formed per mole of aromatic phosphite. The products, some of which are claimed, have the following general formulµ RO-P-(OR1) 2 (RO) 2 -P-OR1 RO-P(OR1)-[-OR11-O-P(OR1)] n -OR (RO) 2 P-[-OR11-O-P(OR1)] n -OR (RO 2 )P-[-OR11-O-P(OR)] n -OR1 (RO) 2 P-[-OR11-O-P(OR)] n -OR R1O-P(OR)-[-OR11-O-P(OR)] n -OR RO-P(OR1)-[-OR11-O-P(OR1)] n -OR1 where R is alkyl or substituted alkyl, R1 is hydroxyalkyl, hydroxyalkoxyalkyl, or substituted alicyclyl, R11 is alkylene, substituted alkylene, alkylenoxy-alkylene or substituted alicyclene, n is an integer. They are used as polymer stabilizers.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_GB1173763A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>GB1173763A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_GB1173763A3</originalsourceid><addsrcrecordid>eNrjZND0zC0oyi9LzU3NKylWKErNSSzJzEtXKMlXcMzJrsxRCMjILy7IyCxJLeZhYE1LzClO5YXS3Azybq4hzh66qQX58anFBYnJqXmpJfHuToaG5sbmZsaOxoRVAACFxyga</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Improvements relating to Alkyl Phosphites</title><source>esp@cenet</source><creator>DAVID FREDERIC WATSON CROSS ; VINCENT OAKES</creator><creatorcontrib>DAVID FREDERIC WATSON CROSS ; VINCENT OAKES</creatorcontrib><description>1,173,763. Alkyl phosphite derivatives. PURE CHEMICALS Ltd. 1 Aug., 1967 [8 Sept., 1966], No. 40116/66. Heading C2C. [Also in Division C3] A process for preparing alkyl phosphite derivatives comprises transesterifying a phosphite of formula (R2O) 3 P, where R2 is alkyl or aryl by liberation of the corresponding alcohol or phenol by reaction with at least two alcohols from the group consisting of alkanols, alkanediols, polyalkylene glycols, and hydrogenated bisphenols, one but not more than one being an alkanol, in the presence of an alkaline or secondary phosphite catalyst, the alcohol being present in such proportions as to enable three moles of alcohol or phenol to be formed per mole of aromatic phosphite. The products, some of which are claimed, have the following general formulµ RO-P-(OR1) 2 (RO) 2 -P-OR1 RO-P(OR1)-[-OR11-O-P(OR1)] n -OR (RO) 2 P-[-OR11-O-P(OR1)] n -OR (RO 2 )P-[-OR11-O-P(OR)] n -OR1 (RO) 2 P-[-OR11-O-P(OR)] n -OR R1O-P(OR)-[-OR11-O-P(OR)] n -OR RO-P(OR1)-[-OR11-O-P(OR1)] n -OR1 where R is alkyl or substituted alkyl, R1 is hydroxyalkyl, hydroxyalkoxyalkyl, or substituted alicyclyl, R11 is alkylene, substituted alkylene, alkylenoxy-alkylene or substituted alicyclene, n is an integer. They are used as polymer stabilizers.</description><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; COMPOSITIONS BASED THEREON ; METALLURGY ; ORGANIC CHEMISTRY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP ; USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</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&amp;date=19691210&amp;DB=EPODOC&amp;CC=GB&amp;NR=1173763A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19691210&amp;DB=EPODOC&amp;CC=GB&amp;NR=1173763A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>DAVID FREDERIC WATSON CROSS</creatorcontrib><creatorcontrib>VINCENT OAKES</creatorcontrib><title>Improvements relating to Alkyl Phosphites</title><description>1,173,763. Alkyl phosphite derivatives. PURE CHEMICALS Ltd. 1 Aug., 1967 [8 Sept., 1966], No. 40116/66. Heading C2C. [Also in Division C3] A process for preparing alkyl phosphite derivatives comprises transesterifying a phosphite of formula (R2O) 3 P, where R2 is alkyl or aryl by liberation of the corresponding alcohol or phenol by reaction with at least two alcohols from the group consisting of alkanols, alkanediols, polyalkylene glycols, and hydrogenated bisphenols, one but not more than one being an alkanol, in the presence of an alkaline or secondary phosphite catalyst, the alcohol being present in such proportions as to enable three moles of alcohol or phenol to be formed per mole of aromatic phosphite. The products, some of which are claimed, have the following general formulµ RO-P-(OR1) 2 (RO) 2 -P-OR1 RO-P(OR1)-[-OR11-O-P(OR1)] n -OR (RO) 2 P-[-OR11-O-P(OR1)] n -OR (RO 2 )P-[-OR11-O-P(OR)] n -OR1 (RO) 2 P-[-OR11-O-P(OR)] n -OR R1O-P(OR)-[-OR11-O-P(OR)] n -OR RO-P(OR1)-[-OR11-O-P(OR1)] n -OR1 where R is alkyl or substituted alkyl, R1 is hydroxyalkyl, hydroxyalkoxyalkyl, or substituted alicyclyl, R11 is alkylene, substituted alkylene, alkylenoxy-alkylene or substituted alicyclene, n is an integer. They are used as polymer stabilizers.</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><subject>USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1969</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZND0zC0oyi9LzU3NKylWKErNSSzJzEtXKMlXcMzJrsxRCMjILy7IyCxJLeZhYE1LzClO5YXS3Azybq4hzh66qQX58anFBYnJqXmpJfHuToaG5sbmZsaOxoRVAACFxyga</recordid><startdate>19691210</startdate><enddate>19691210</enddate><creator>DAVID FREDERIC WATSON CROSS</creator><creator>VINCENT OAKES</creator><scope>EVB</scope></search><sort><creationdate>19691210</creationdate><title>Improvements relating to Alkyl Phosphites</title><author>DAVID FREDERIC WATSON CROSS ; VINCENT OAKES</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GB1173763A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</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>COMPOSITIONS BASED THEREON</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><topic>USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS</topic><toplevel>online_resources</toplevel><creatorcontrib>DAVID FREDERIC WATSON CROSS</creatorcontrib><creatorcontrib>VINCENT OAKES</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>DAVID FREDERIC WATSON CROSS</au><au>VINCENT OAKES</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Improvements relating to Alkyl Phosphites</title><date>1969-12-10</date><risdate>1969</risdate><abstract>1,173,763. Alkyl phosphite derivatives. PURE CHEMICALS Ltd. 1 Aug., 1967 [8 Sept., 1966], No. 40116/66. Heading C2C. [Also in Division C3] A process for preparing alkyl phosphite derivatives comprises transesterifying a phosphite of formula (R2O) 3 P, where R2 is alkyl or aryl by liberation of the corresponding alcohol or phenol by reaction with at least two alcohols from the group consisting of alkanols, alkanediols, polyalkylene glycols, and hydrogenated bisphenols, one but not more than one being an alkanol, in the presence of an alkaline or secondary phosphite catalyst, the alcohol being present in such proportions as to enable three moles of alcohol or phenol to be formed per mole of aromatic phosphite. The products, some of which are claimed, have the following general formulµ RO-P-(OR1) 2 (RO) 2 -P-OR1 RO-P(OR1)-[-OR11-O-P(OR1)] n -OR (RO) 2 P-[-OR11-O-P(OR1)] n -OR (RO 2 )P-[-OR11-O-P(OR)] n -OR1 (RO) 2 P-[-OR11-O-P(OR)] n -OR R1O-P(OR)-[-OR11-O-P(OR)] n -OR RO-P(OR1)-[-OR11-O-P(OR1)] n -OR1 where R is alkyl or substituted alkyl, R1 is hydroxyalkyl, hydroxyalkoxyalkyl, or substituted alicyclyl, R11 is alkylene, substituted alkylene, alkylenoxy-alkylene or substituted alicyclene, n is an integer. They are used as polymer stabilizers.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_GB1173763A
source esp@cenet
subjects ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
COMPOSITIONS BASED THEREON
METALLURGY
ORGANIC CHEMISTRY
ORGANIC MACROMOLECULAR COMPOUNDS
THEIR PREPARATION OR CHEMICAL WORKING-UP
USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUBSTANCES ASCOMPOUNDING INGREDIENTS
title Improvements relating to Alkyl Phosphites
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T23%3A23%3A58IST&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=DAVID%20FREDERIC%20WATSON%20CROSS&rft.date=1969-12-10&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EGB1173763A%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