Preparation method for efficiently synthesizing ferrocene tetrafluoroborate
The invention relates to the technical field of ferrocene tetrafluoroborate, and discloses a preparation method for efficiently synthesizing ferrocene tetrafluoroborate, which comprises the following steps: at normal temperature, adding ferrocene and p-benzoquinone into a round-bottom flask filled w...
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 | XU YINGYU WU GUOYIN ZHANG LEBO NIU ZUORAN |
description | The invention relates to the technical field of ferrocene tetrafluoroborate, and discloses a preparation method for efficiently synthesizing ferrocene tetrafluoroborate, which comprises the following steps: at normal temperature, adding ferrocene and p-benzoquinone into a round-bottom flask filled with an absolute ether solution, stirring for 20-50 minutes, then continuously dropwise adding a tetrafluoroborate-diethyl ether complex into the round-bottom flask, stirring, filtering, washing, and drying to obtain the ferrocene tetrafluoroborate. The preparation method comprises the following steps: reacting for 30-60 minutes to generate a bluish violet precipitate in a round-bottom flask, filtering a solution obtained in the round-bottom flask to obtain the bluish violet precipitate, stirring and dissolving the obtained bluish violet precipitate in a round-bottom beaker filled with acetone, then adding absolute ether, separating out the bluish violet precipitate, repeating the step for 3-6 times, filtering the o |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN117069774A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN117069774A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN117069774A3</originalsourceid><addsrcrecordid>eNrjZPAOKEotSCxKLMnMz1PITS3JyE9RSMsvUkhNS8tMzkzNK8mpVCiuzCvJSC3OrMrMS1dISy0qyk9OzUtVKEktKUpMyynNL8pPygeakMrDwJqWmFOcyguluRkU3VxDnD10Uwvy41OLCxJB2krinf0MDc0NzCzNzU0cjYlRAwAO3jcB</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Preparation method for efficiently synthesizing ferrocene tetrafluoroborate</title><source>esp@cenet</source><creator>XU YINGYU ; WU GUOYIN ; ZHANG LEBO ; NIU ZUORAN</creator><creatorcontrib>XU YINGYU ; WU GUOYIN ; ZHANG LEBO ; NIU ZUORAN</creatorcontrib><description>The invention relates to the technical field of ferrocene tetrafluoroborate, and discloses a preparation method for efficiently synthesizing ferrocene tetrafluoroborate, which comprises the following steps: at normal temperature, adding ferrocene and p-benzoquinone into a round-bottom flask filled with an absolute ether solution, stirring for 20-50 minutes, then continuously dropwise adding a tetrafluoroborate-diethyl ether complex into the round-bottom flask, stirring, filtering, washing, and drying to obtain the ferrocene tetrafluoroborate. The preparation method comprises the following steps: reacting for 30-60 minutes to generate a bluish violet precipitate in a round-bottom flask, filtering a solution obtained in the round-bottom flask to obtain the bluish violet precipitate, stirring and dissolving the obtained bluish violet precipitate in a round-bottom beaker filled with acetone, then adding absolute ether, separating out the bluish violet precipitate, repeating the step for 3-6 times, filtering the o</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>2023</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=20231117&DB=EPODOC&CC=CN&NR=117069774A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20231117&DB=EPODOC&CC=CN&NR=117069774A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>XU YINGYU</creatorcontrib><creatorcontrib>WU GUOYIN</creatorcontrib><creatorcontrib>ZHANG LEBO</creatorcontrib><creatorcontrib>NIU ZUORAN</creatorcontrib><title>Preparation method for efficiently synthesizing ferrocene tetrafluoroborate</title><description>The invention relates to the technical field of ferrocene tetrafluoroborate, and discloses a preparation method for efficiently synthesizing ferrocene tetrafluoroborate, which comprises the following steps: at normal temperature, adding ferrocene and p-benzoquinone into a round-bottom flask filled with an absolute ether solution, stirring for 20-50 minutes, then continuously dropwise adding a tetrafluoroborate-diethyl ether complex into the round-bottom flask, stirring, filtering, washing, and drying to obtain the ferrocene tetrafluoroborate. The preparation method comprises the following steps: reacting for 30-60 minutes to generate a bluish violet precipitate in a round-bottom flask, filtering a solution obtained in the round-bottom flask to obtain the bluish violet precipitate, stirring and dissolving the obtained bluish violet precipitate in a round-bottom beaker filled with acetone, then adding absolute ether, separating out the bluish violet precipitate, repeating the step for 3-6 times, filtering the o</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>2023</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPAOKEotSCxKLMnMz1PITS3JyE9RSMsvUkhNS8tMzkzNK8mpVCiuzCvJSC3OrMrMS1dISy0qyk9OzUtVKEktKUpMyynNL8pPygeakMrDwJqWmFOcyguluRkU3VxDnD10Uwvy41OLCxJB2krinf0MDc0NzCzNzU0cjYlRAwAO3jcB</recordid><startdate>20231117</startdate><enddate>20231117</enddate><creator>XU YINGYU</creator><creator>WU GUOYIN</creator><creator>ZHANG LEBO</creator><creator>NIU ZUORAN</creator><scope>EVB</scope></search><sort><creationdate>20231117</creationdate><title>Preparation method for efficiently synthesizing ferrocene tetrafluoroborate</title><author>XU YINGYU ; WU GUOYIN ; ZHANG LEBO ; NIU ZUORAN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN117069774A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2023</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>XU YINGYU</creatorcontrib><creatorcontrib>WU GUOYIN</creatorcontrib><creatorcontrib>ZHANG LEBO</creatorcontrib><creatorcontrib>NIU ZUORAN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>XU YINGYU</au><au>WU GUOYIN</au><au>ZHANG LEBO</au><au>NIU ZUORAN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Preparation method for efficiently synthesizing ferrocene tetrafluoroborate</title><date>2023-11-17</date><risdate>2023</risdate><abstract>The invention relates to the technical field of ferrocene tetrafluoroborate, and discloses a preparation method for efficiently synthesizing ferrocene tetrafluoroborate, which comprises the following steps: at normal temperature, adding ferrocene and p-benzoquinone into a round-bottom flask filled with an absolute ether solution, stirring for 20-50 minutes, then continuously dropwise adding a tetrafluoroborate-diethyl ether complex into the round-bottom flask, stirring, filtering, washing, and drying to obtain the ferrocene tetrafluoroborate. The preparation method comprises the following steps: reacting for 30-60 minutes to generate a bluish violet precipitate in a round-bottom flask, filtering a solution obtained in the round-bottom flask to obtain the bluish violet precipitate, stirring and dissolving the obtained bluish violet precipitate in a round-bottom beaker filled with acetone, then adding absolute ether, separating out the bluish violet precipitate, repeating the step for 3-6 times, filtering the o</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | chi ; eng |
recordid | cdi_epo_espacenet_CN117069774A |
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 | Preparation method for efficiently synthesizing ferrocene tetrafluoroborate |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T22%3A57%3A54IST&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=XU%20YINGYU&rft.date=2023-11-17&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN117069774A%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 |