Investigation of the catalytic activity of metallic copper and copper dispersed SiO2 for the reductive acetylation of aromatic nitro compounds

N -Arylacetamides such as acetaminophen are important systems in medicinal chemistry. Reductive acetylation of nitroarenes is noted to be an efficient route for their preparation. Protocols were developed for one-pot reductive acetylation of nitroarenes in the presence of various catalysts under var...

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Veröffentlicht in:Research on chemical intermediates 2022, Vol.48 (5), p.1939-1952
Hauptverfasser: Govindaraj, Devi, Gopal, Buvaneswari
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description N -Arylacetamides such as acetaminophen are important systems in medicinal chemistry. Reductive acetylation of nitroarenes is noted to be an efficient route for their preparation. Protocols were developed for one-pot reductive acetylation of nitroarenes in the presence of various catalysts under varied conditions. Current work studied the catalytic effect of metallic copper and supported copper systems towards the reductive acetylation of nitroarenes under mild condition. The influence of the supporting materials such as SiO 2 , Al 2 O 3 , TiO 2 and HAp (hydroxyapatite) was studied by comparing the activity of Cu/SiO 2 with that of Cu/TiO 2 , Cu/Al 2 O 3 and Cu/HAp. Cu/SiO 2 system emerged out as an efficient catalyst. In the first part of the reaction of reduction of nitrobenzene to aniline, both 4 wt% Cu–Al 2 O 3 and 4 wt% Cu–HAp lead to partial conversion till the formation of azoxybenzene, whereas 4 wt% Cu–TiO 2 showed 31% conversion of aniline. However, with 4 wt% Cu–SiO 2 , 100% conversion of aniline was achieved. Acetylation of the system afforded 97% yield of N -phenylacetamide. The activity of the catalyst was also tested for selected nitroarenes. Characterization by powder XRD, XPS, TEM, BET measurements, TPR study assisted in demonstrating the efficacy of SiO 2 -supported Cu.
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Reductive acetylation of nitroarenes is noted to be an efficient route for their preparation. Protocols were developed for one-pot reductive acetylation of nitroarenes in the presence of various catalysts under varied conditions. Current work studied the catalytic effect of metallic copper and supported copper systems towards the reductive acetylation of nitroarenes under mild condition. The influence of the supporting materials such as SiO 2 , Al 2 O 3 , TiO 2 and HAp (hydroxyapatite) was studied by comparing the activity of Cu/SiO 2 with that of Cu/TiO 2 , Cu/Al 2 O 3 and Cu/HAp. Cu/SiO 2 system emerged out as an efficient catalyst. In the first part of the reaction of reduction of nitrobenzene to aniline, both 4 wt% Cu–Al 2 O 3 and 4 wt% Cu–HAp lead to partial conversion till the formation of azoxybenzene, whereas 4 wt% Cu–TiO 2 showed 31% conversion of aniline. However, with 4 wt% Cu–SiO 2 , 100% conversion of aniline was achieved. Acetylation of the system afforded 97% yield of N -phenylacetamide. The activity of the catalyst was also tested for selected nitroarenes. 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Reductive acetylation of nitroarenes is noted to be an efficient route for their preparation. Protocols were developed for one-pot reductive acetylation of nitroarenes in the presence of various catalysts under varied conditions. Current work studied the catalytic effect of metallic copper and supported copper systems towards the reductive acetylation of nitroarenes under mild condition. The influence of the supporting materials such as SiO 2 , Al 2 O 3 , TiO 2 and HAp (hydroxyapatite) was studied by comparing the activity of Cu/SiO 2 with that of Cu/TiO 2 , Cu/Al 2 O 3 and Cu/HAp. Cu/SiO 2 system emerged out as an efficient catalyst. In the first part of the reaction of reduction of nitrobenzene to aniline, both 4 wt% Cu–Al 2 O 3 and 4 wt% Cu–HAp lead to partial conversion till the formation of azoxybenzene, whereas 4 wt% Cu–TiO 2 showed 31% conversion of aniline. However, with 4 wt% Cu–SiO 2 , 100% conversion of aniline was achieved. Acetylation of the system afforded 97% yield of N -phenylacetamide. The activity of the catalyst was also tested for selected nitroarenes. Characterization by powder XRD, XPS, TEM, BET measurements, TPR study assisted in demonstrating the efficacy of SiO 2 -supported Cu.</description><subject>Acetylation</subject><subject>Aluminum oxide</subject><subject>Aniline</subject><subject>Aromatic compounds</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Conversion</subject><subject>Copper</subject><subject>Hydroxyapatite</subject><subject>Inorganic Chemistry</subject><subject>Nitro compounds</subject><subject>Nitrobenzene</subject><subject>Physical Chemistry</subject><subject>Silicon dioxide</subject><subject>Titanium dioxide</subject><issn>0922-6168</issn><issn>1568-5675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kMtOwzAQRS0EEqXwA6wisQ6Mnfi1RBWPSkgsgLXlOE5x1cbBdivlJ_hm3JbHjtWMZu49V7oIXWK4xgD8JmKMWV0CISXUHKpyPEITTJkoKeP0GE1A5hfDTJyisxiXAJgKARP0Oe-3Nia30Mn5vvBdkd5tYXTSqzE5U2iT3NalcfdZ23xd5aPxw2BDofv2Z21dzCPatnhxz6TofNhzgm03O4DNHJvG1W-IDn6td_zepeAzZT34Td_Gc3TS6VW0F99zit7u715nj-XT88N8dvtUGgKQSgkdE6YCA5RIJhuOKQgtWduamre6qYS01gCWQlvb1BWtmga4rjknkjQMqim6OnCH4D82uQC19JvQ50hFGKVUSEJ5VpGDygQfY7CdGoJb6zAqDGrXuzr0rnLvat-7GrOpOphiFvcLG_7Q_7i-ALiciRk</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Govindaraj, Devi</creator><creator>Gopal, Buvaneswari</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-9578-6020</orcidid></search><sort><creationdate>2022</creationdate><title>Investigation of the catalytic activity of metallic copper and copper dispersed SiO2 for the reductive acetylation of aromatic nitro compounds</title><author>Govindaraj, Devi ; Gopal, Buvaneswari</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c200t-90f68c30c052969b71508a96ddc47dab389eec0198aeeb4353bb07a477292b603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Acetylation</topic><topic>Aluminum oxide</topic><topic>Aniline</topic><topic>Aromatic compounds</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Conversion</topic><topic>Copper</topic><topic>Hydroxyapatite</topic><topic>Inorganic Chemistry</topic><topic>Nitro compounds</topic><topic>Nitrobenzene</topic><topic>Physical Chemistry</topic><topic>Silicon dioxide</topic><topic>Titanium dioxide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Govindaraj, Devi</creatorcontrib><creatorcontrib>Gopal, Buvaneswari</creatorcontrib><collection>CrossRef</collection><jtitle>Research on chemical intermediates</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Govindaraj, Devi</au><au>Gopal, Buvaneswari</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of the catalytic activity of metallic copper and copper dispersed SiO2 for the reductive acetylation of aromatic nitro compounds</atitle><jtitle>Research on chemical intermediates</jtitle><stitle>Res Chem Intermed</stitle><date>2022</date><risdate>2022</risdate><volume>48</volume><issue>5</issue><spage>1939</spage><epage>1952</epage><pages>1939-1952</pages><issn>0922-6168</issn><eissn>1568-5675</eissn><abstract>N -Arylacetamides such as acetaminophen are important systems in medicinal chemistry. 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subjects Acetylation
Aluminum oxide
Aniline
Aromatic compounds
Catalysis
Catalysts
Catalytic activity
Chemistry
Chemistry and Materials Science
Conversion
Copper
Hydroxyapatite
Inorganic Chemistry
Nitro compounds
Nitrobenzene
Physical Chemistry
Silicon dioxide
Titanium dioxide
title Investigation of the catalytic activity of metallic copper and copper dispersed SiO2 for the reductive acetylation of aromatic nitro compounds
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