{"id":527,"date":"2018-11-26T15:59:42","date_gmt":"2018-11-26T15:59:42","guid":{"rendered":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/?post_type=chapter&#038;p=527"},"modified":"2021-03-19T13:40:55","modified_gmt":"2021-03-19T13:40:55","slug":"15-6-examples-of-multistep-synthesis-chemistry-libretexts","status":"publish","type":"chapter","link":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/chapter\/15-6-examples-of-multistep-synthesis-chemistry-libretexts\/","title":{"raw":"15.6 Worked Examples","rendered":"15.6 Worked Examples"},"content":{"raw":"<header class=\"elm-header\">\r\n<div class=\"elm-header-custom\">\r\n<div class=\"mt-container-secondary\"><span style=\"color: #000000\"><span style=\"font-size: 1em\"> From benzene make\u00a0<\/span><em style=\"font-size: 1em;font-weight: 600\">m<\/em><span style=\"font-size: 1em\">-bromoaniline<\/span><\/span><\/div>\r\n<\/div>\r\n<\/header><article id=\"elm-main-content\" class=\"elm-content-container\"><section class=\"mt-content-container\">\r\n<div id=\"section_1\" class=\"mt-section\">\r\n\r\nIn this reaction three reactions are required.\r\n<ol>\r\n \t<li>A nitration<\/li>\r\n \t<li>A conversion from the nitro group to an amine<\/li>\r\n \t<li>A bromination<\/li>\r\n<\/ol>\r\nBecause the end product is meta a meta directing group must be utilized. Of the nitro, bromine, and amine group, only the nitro group is meta direction. This means that the first step need to be the nitration and not the bromination. Also, the conversion of the nitro group to an amine must occur last because the amine group is ortho\/para direction.\r\n\r\n<img class=\"wp-image-3177 aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3773\/2018\/11\/19133307\/mBromoanilineLibretexts.png\" alt=\"Prep of m-Nitroaniline by nitration, bromination then reduction\" width=\"409\" height=\"312\" \/>\r\n\r\n<span style=\"color: #000000\"><span style=\"font-size: 1em\">From benzene make <\/span><em style=\"font-size: 1em;font-weight: 600\">p<\/em><span style=\"font-size: 1em\">-nitropropylbenzene <\/span><span id=\"selectionBoundary_1430110002815_17477731805340657\" class=\"rangySelectionBoundary\" style=\"font-size: 1em\">:<\/span><\/span>\r\n\r\n<\/div>\r\n<div id=\"section_2\" class=\"mt-section\">\r\n\r\nIn this reaction three reactions are required.\r\n<ol>\r\n \t<li>A Friedel Crafts acylation<\/li>\r\n \t<li>A conversion from the acyl group to an alkane<\/li>\r\n \t<li>A nitration<\/li>\r\n<\/ol>\r\nBecause the propyl group has more than two carbons, it must be added in two steps. A Friedel Crafts acylation followed by a Clemmensen Reduction. Remeber that Friedel Crafts reactions are hindered if the benzene ring is strongly deactivated. This means that the acyl group must go on first. Because the end product is para a para directing group must be utilized. Of the nitro, acyl, and alkane group, only the alkane group is meta direction. This means that the acyl group must be converted to an alkane prior to the nitration step.\r\n\r\n<\/div>\r\n<div id=\"section_3\" class=\"mt-section\">\r\n\r\n<img class=\"size-full wp-image-3176 aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3773\/2018\/11\/19133251\/pNitroPropylbenzeneLibretexts.png\" alt=\"A multistep synthesis of p-nitropropylbenzene via FC acylation, reduction and nitration\" width=\"502\" height=\"395\" \/>\r\n<h3 class=\"editable\">Contributors<\/h3>\r\n<ul>\r\n \t<li>Prof. Steven Farmer (<a class=\"external\" title=\"http:\/\/www.sonoma.edu\" href=\"http:\/\/www.sonoma.edu\" target=\"_blank\" rel=\"external nofollow noopener\">Sonoma State University<\/a>)<\/li>\r\n<\/ul>\r\n<\/div>\r\n<\/section><\/article>","rendered":"<header class=\"elm-header\">\n<div class=\"elm-header-custom\">\n<div class=\"mt-container-secondary\"><span style=\"color: #000000\"><span style=\"font-size: 1em\"> From benzene make\u00a0<\/span><em style=\"font-size: 1em;font-weight: 600\">m<\/em><span style=\"font-size: 1em\">-bromoaniline<\/span><\/span><\/div>\n<\/div>\n<\/header>\n<article id=\"elm-main-content\" class=\"elm-content-container\">\n<section class=\"mt-content-container\">\n<div id=\"section_1\" class=\"mt-section\">\n<p>In this reaction three reactions are required.<\/p>\n<ol>\n<li>A nitration<\/li>\n<li>A conversion from the nitro group to an amine<\/li>\n<li>A bromination<\/li>\n<\/ol>\n<p>Because the end product is meta a meta directing group must be utilized. Of the nitro, bromine, and amine group, only the nitro group is meta direction. This means that the first step need to be the nitration and not the bromination. Also, the conversion of the nitro group to an amine must occur last because the amine group is ortho\/para direction.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-3177 aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3773\/2018\/11\/19133307\/mBromoanilineLibretexts.png\" alt=\"Prep of m-Nitroaniline by nitration, bromination then reduction\" width=\"409\" height=\"312\" \/><\/p>\n<p><span style=\"color: #000000\"><span style=\"font-size: 1em\">From benzene make <\/span><em style=\"font-size: 1em;font-weight: 600\">p<\/em><span style=\"font-size: 1em\">-nitropropylbenzene <\/span><span id=\"selectionBoundary_1430110002815_17477731805340657\" class=\"rangySelectionBoundary\" style=\"font-size: 1em\">:<\/span><\/span><\/p>\n<\/div>\n<div id=\"section_2\" class=\"mt-section\">\n<p>In this reaction three reactions are required.<\/p>\n<ol>\n<li>A Friedel Crafts acylation<\/li>\n<li>A conversion from the acyl group to an alkane<\/li>\n<li>A nitration<\/li>\n<\/ol>\n<p>Because the propyl group has more than two carbons, it must be added in two steps. A Friedel Crafts acylation followed by a Clemmensen Reduction. Remeber that Friedel Crafts reactions are hindered if the benzene ring is strongly deactivated. This means that the acyl group must go on first. Because the end product is para a para directing group must be utilized. Of the nitro, acyl, and alkane group, only the alkane group is meta direction. This means that the acyl group must be converted to an alkane prior to the nitration step.<\/p>\n<\/div>\n<div id=\"section_3\" class=\"mt-section\">\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-3176 aligncenter\" src=\"https:\/\/s3-us-west-2.amazonaws.com\/courses-images\/wp-content\/uploads\/sites\/3773\/2018\/11\/19133251\/pNitroPropylbenzeneLibretexts.png\" alt=\"A multistep synthesis of p-nitropropylbenzene via FC acylation, reduction and nitration\" width=\"502\" height=\"395\" \/><\/p>\n<h3 class=\"editable\">Contributors<\/h3>\n<ul>\n<li>Prof. Steven Farmer (<a class=\"external\" title=\"http:\/\/www.sonoma.edu\" href=\"http:\/\/www.sonoma.edu\" target=\"_blank\" rel=\"external nofollow noopener\">Sonoma State University<\/a>)<\/li>\n<\/ul>\n<\/div>\n<\/section>\n<\/article>\n\n\t\t\t <section class=\"citations-section\" role=\"contentinfo\">\n\t\t\t <h3>Candela Citations<\/h3>\n\t\t\t\t\t <div>\n\t\t\t\t\t\t <div id=\"citation-list-527\">\n\t\t\t\t\t\t\t <div class=\"licensing\"><div class=\"license-attribution-dropdown-subheading\">CC licensed content, Shared previously<\/div><ul class=\"citation-list\"><li>18.15 Examples of Multistep Synthesis. <strong>Authored by<\/strong>: Prof. Steven Farmer . <strong>Provided by<\/strong>: Sonoma State University. <strong>Located at<\/strong>: <a target=\"_blank\" href=\"https:\/\/chem.libretexts.org\/LibreTexts\/University_of_Illinois%2C_Springfield\/UIS%3A_CHE_269_-_Organic_Chemistry_II_(Morsch)\/Chapters\/Chapter_18%3A_Electrophilic_Aromatic_Substitution\/18.15_Examples_of_Multistep_Synthesis\">https:\/\/chem.libretexts.org\/LibreTexts\/University_of_Illinois%2C_Springfield\/UIS%3A_CHE_269_-_Organic_Chemistry_II_(Morsch)\/Chapters\/Chapter_18%3A_Electrophilic_Aromatic_Substitution\/18.15_Examples_of_Multistep_Synthesis<\/a>. <strong>Project<\/strong>: Chemistry LibreTexts . <strong>License<\/strong>: <em><a target=\"_blank\" rel=\"license\" href=\"https:\/\/creativecommons.org\/licenses\/by-nc-sa\/4.0\/\">CC BY-NC-SA: Attribution-NonCommercial-ShareAlike<\/a><\/em><\/li><\/ul><\/div>\n\t\t\t\t\t\t <\/div>\n\t\t\t\t\t <\/div>\n\t\t\t <\/section>","protected":false},"author":311,"menu_order":4,"template":"","meta":{"_candela_citation":"[{\"type\":\"cc\",\"description\":\"18.15 Examples of Multistep Synthesis\",\"author\":\"Prof. Steven Farmer \",\"organization\":\"Sonoma State University\",\"url\":\"https:\/\/chem.libretexts.org\/LibreTexts\/University_of_Illinois%2C_Springfield\/UIS%3A_CHE_269_-_Organic_Chemistry_II_(Morsch)\/Chapters\/Chapter_18%3A_Electrophilic_Aromatic_Substitution\/18.15_Examples_of_Multistep_Synthesis\",\"project\":\"Chemistry LibreTexts \",\"license\":\"cc-by-nc-sa\",\"license_terms\":\"\"}]","CANDELA_OUTCOMES_GUID":"","pb_show_title":"on","pb_short_title":"","pb_subtitle":"","pb_authors":[],"pb_section_license":""},"chapter-type":[],"contributor":[],"license":[],"class_list":["post-527","chapter","type-chapter","status-publish","hentry"],"part":507,"_links":{"self":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/pressbooks\/v2\/chapters\/527","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/pressbooks\/v2\/chapters"}],"about":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/wp\/v2\/types\/chapter"}],"author":[{"embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/wp\/v2\/users\/311"}],"version-history":[{"count":7,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/pressbooks\/v2\/chapters\/527\/revisions"}],"predecessor-version":[{"id":3179,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/pressbooks\/v2\/chapters\/527\/revisions\/3179"}],"part":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/pressbooks\/v2\/parts\/507"}],"metadata":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/pressbooks\/v2\/chapters\/527\/metadata\/"}],"wp:attachment":[{"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/wp\/v2\/media?parent=527"}],"wp:term":[{"taxonomy":"chapter-type","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/pressbooks\/v2\/chapter-type?post=527"},{"taxonomy":"contributor","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/wp\/v2\/contributor?post=527"},{"taxonomy":"license","embeddable":true,"href":"https:\/\/courses.lumenlearning.com\/suny-potsdam-organicchemistry2\/wp-json\/wp\/v2\/license?post=527"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}