Preparation of straight chain aldehydes

Preparation of straight chain aldehydes

Straight chain aldehydes are prepared from straight chain olefins of about 3 to 20 carbon atoms by catalytic hydroformylation with carbon monoxide and hydrogen in the presence of cobalt catalyst and in the presence of soluble primary, secondary or tertiary aliphatic, or cycloaliphatic amine modifier...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: WILKES, JOHN B
Format: Patent
Sprache:eng
Schlagworte:
ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
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 WILKES
JOHN B
description Straight chain aldehydes are prepared from straight chain olefins of about 3 to 20 carbon atoms by catalytic hydroformylation with carbon monoxide and hydrogen in the presence of cobalt catalyst and in the presence of soluble primary, secondary or tertiary aliphatic, or cycloaliphatic amine modifier of 1 to 12 carbon atoms.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_US4096188A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>US4096188A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_US4096188A3</originalsourceid><addsrcrecordid>eNrjZFAPKEotSCxKLMnMz1PIT1MoLilKzEzPKFFIzkjMzFNIzElJzahMSS3mYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxocEmBpZmhhYWjsaEVQAAGVUndg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Preparation of straight chain aldehydes</title><source>esp@cenet</source><creator>WILKES; JOHN B</creator><creatorcontrib>WILKES; JOHN B</creatorcontrib><description>Straight chain aldehydes are prepared from straight chain olefins of about 3 to 20 carbon atoms by catalytic hydroformylation with carbon monoxide and hydrogen in the presence of cobalt catalyst and in the presence of soluble primary, secondary or tertiary aliphatic, or cycloaliphatic amine modifier of 1 to 12 carbon atoms.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1978</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=19780620&amp;DB=EPODOC&amp;CC=US&amp;NR=4096188A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19780620&amp;DB=EPODOC&amp;CC=US&amp;NR=4096188A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>WILKES; JOHN B</creatorcontrib><title>Preparation of straight chain aldehydes</title><description>Straight chain aldehydes are prepared from straight chain olefins of about 3 to 20 carbon atoms by catalytic hydroformylation with carbon monoxide and hydrogen in the presence of cobalt catalyst and in the presence of soluble primary, secondary or tertiary aliphatic, or cycloaliphatic amine modifier of 1 to 12 carbon atoms.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1978</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFAPKEotSCxKLMnMz1PIT1MoLilKzEzPKFFIzkjMzFNIzElJzahMSS3mYWBNS8wpTuWF0twM8m6uIc4euqkF-fGpxQWJyal5qSXxocEmBpZmhhYWjsaEVQAAGVUndg</recordid><startdate>19780620</startdate><enddate>19780620</enddate><creator>WILKES; JOHN B</creator><scope>EVB</scope></search><sort><creationdate>19780620</creationdate><title>Preparation of straight chain aldehydes</title><author>WILKES; JOHN B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US4096188A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1978</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>WILKES; JOHN B</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>WILKES; JOHN B</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Preparation of straight chain aldehydes</title><date>1978-06-20</date><risdate>1978</risdate><abstract>Straight chain aldehydes are prepared from straight chain olefins of about 3 to 20 carbon atoms by catalytic hydroformylation with carbon monoxide and hydrogen in the presence of cobalt catalyst and in the presence of soluble primary, secondary or tertiary aliphatic, or cycloaliphatic amine modifier of 1 to 12 carbon atoms.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_US4096188A
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
title Preparation of straight chain aldehydes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T00%3A17%3A33IST&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=WILKES;%20JOHN%20B&rft.date=1978-06-20&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EUS4096188A%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