{"id":9001,"date":"2024-01-25T03:04:56","date_gmt":"2024-01-25T03:04:56","guid":{"rendered":"https:\/\/chemistryscore.com\/?page_id=9001---53fb2fe0-db30-481a-bb36-516e070008e1"},"modified":"2024-01-25T03:04:58","modified_gmt":"2024-01-25T03:04:58","slug":"conversion-ketones-gilman-reagents","status":"publish","type":"post","link":"https:\/\/chemistryscore.com\/conversion-ketones-gilman-reagents\/","title":{"rendered":"Conversion to ketones [Gilman reagents]"},"content":{"rendered":"\t\t
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Conversion to ketones [Gilman reagents]<\/h1>

Conversion to ketones [Gilman reagents] Definition:<\/h2>

Addition of organocuprates <\/b>(Gilman reagents<\/b>) to acid chlorides<\/b> results in ketones<\/b>.<\/p>

\"\"<\/p>

Conversion to ketones [Gilman reagents] Explained:<\/h2>

Organometallic reagents may attack the carbonyl group of acyl halides to give the corresponding ketones. Organolithiums and Grignards are relatively unselective and products from this reactions may further react. Ketone formation is best achieved by using organocuprates <\/b>(Gilman reagents<\/b>), which are more selective <\/b>than organolithium and Grignard reagents and do not add<\/b> to the product ketone. This reaction results in a nucleophilic substitution<\/b> of an alkyl group for the leaving group (chloride), forming one new carbon-carbon bond<\/b>.<\/p>

Mechanism of Addition of Gilman to Acyl Halides<\/h3>

This mechanism consists of two steps. In the first step<\/b>, one of the methyl groups of organocuprate function as a nucleophile and attacks carbonyl carbon (Remeber: whenever a carbon is attached to a metal it has a negative charge<\/em>). \u03c0 bond will break and in the next step<\/b>, this bond will re-form by expelling a good leaving group (chloride ion). And the final ketone will be formed.<\/p>

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Conversion to ketones [Gilman reagents] Conversion to ketones [Gilman reagents] Definition: Addition of organocuprates (Gilman reagents) to acid chlorides results in ketones. Conversion to ketones [Gilman reagents] Explained: Organometallic reagents may attack the carbonyl group of acyl halides to give the corresponding ketones. Organolithiums and Grignards are relatively unselective and products from this reactions may […]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"elementor_header_footer","format":"standard","meta":{"ocean_post_layout":"","ocean_both_sidebars_style":"","ocean_both_sidebars_content_width":0,"ocean_both_sidebars_sidebars_width":0,"ocean_sidebar":"0","ocean_second_sidebar":"0","ocean_disable_margins":"enable","ocean_add_body_class":"","ocean_shortcode_before_top_bar":"","ocean_shortcode_after_top_bar":"","ocean_shortcode_before_header":"","ocean_shortcode_after_header":"","ocean_has_shortcode":"","ocean_shortcode_after_title":"","ocean_shortcode_before_footer_widgets":"","ocean_shortcode_after_footer_widgets":"","ocean_shortcode_before_footer_bottom":"","ocean_shortcode_after_footer_bottom":"","ocean_display_top_bar":"default","ocean_display_header":"default","ocean_header_style":"","ocean_center_header_left_menu":"0","ocean_custom_header_template":"0","ocean_custom_logo":0,"ocean_custom_retina_logo":0,"ocean_custom_logo_max_width":0,"ocean_custom_logo_tablet_max_width":0,"ocean_custom_logo_mobile_max_width":0,"ocean_custom_logo_max_height":0,"ocean_custom_logo_tablet_max_height":0,"ocean_custom_logo_mobile_max_height":0,"ocean_header_custom_menu":"0","ocean_menu_typo_font_family":"0","ocean_menu_typo_font_subset":"","ocean_menu_typo_font_size":0,"ocean_menu_typo_font_size_tablet":0,"ocean_menu_typo_font_size_mobile":0,"ocean_menu_typo_font_size_unit":"px","ocean_menu_typo_font_weight":"","ocean_menu_typo_font_weight_tablet":"","ocean_menu_typo_font_weight_mobile":"","ocean_menu_typo_transform":"","ocean_menu_typo_transform_tablet":"","ocean_menu_typo_transform_mobile":"","ocean_menu_typo_line_height":0,"ocean_menu_typo_line_height_tablet":0,"ocean_menu_typo_line_height_mobile":0,"ocean_menu_typo_line_height_unit":"","ocean_menu_typo_spacing":0,"ocean_menu_typo_spacing_tablet":0,"ocean_menu_typo_spacing_mobile":0,"ocean_menu_typo_spacing_unit":"","ocean_menu_link_color":"","ocean_menu_link_color_hover":"","ocean_menu_link_color_active":"","ocean_menu_link_background":"","ocean_menu_link_hover_background":"","ocean_menu_link_active_background":"","ocean_menu_social_links_bg":"","ocean_menu_social_hover_links_bg":"","ocean_menu_social_links_color":"","ocean_menu_social_hover_links_color":"","ocean_disable_title":"default","ocean_disable_heading":"on","ocean_post_title":"","ocean_post_subheading":"","ocean_post_title_style":"","ocean_post_title_background_color":"","ocean_post_title_background":0,"ocean_post_title_bg_image_position":"","ocean_post_title_bg_image_attachment":"","ocean_post_title_bg_image_repeat":"","ocean_post_title_bg_image_size":"","ocean_post_title_height":0,"ocean_post_title_bg_overlay":0.5,"ocean_post_title_bg_overlay_color":"","ocean_disable_breadcrumbs":"default","ocean_breadcrumbs_color":"","ocean_breadcrumbs_separator_color":"","ocean_breadcrumbs_links_color":"","ocean_breadcrumbs_links_hover_color":"","ocean_display_footer_widgets":"default","ocean_display_footer_bottom":"default","ocean_custom_footer_template":"0","_jetpack_memberships_contains_paid_content":false,"ocean_post_oembed":"","ocean_post_self_hosted_media":"","ocean_post_video_embed":"","ocean_link_format":"","ocean_link_format_target":"self","ocean_quote_format":"","ocean_quote_format_link":"post","ocean_gallery_link_images":"off","ocean_gallery_id":[],"footnotes":""},"categories":[5634],"tags":[],"jetpack_sharing_enabled":true,"jetpack_featured_media_url":"","yoast_head":"\nConversion to ketones [Gilman reagents] - ChemistryScore<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/chemistryscore.com\/conversion-ketones-gilman-reagents\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Conversion to ketones [Gilman reagents] - ChemistryScore\" \/>\n<meta property=\"og:description\" content=\"Conversion to ketones [Gilman reagents] Conversion to ketones [Gilman reagents] Definition: Addition of organocuprates (Gilman reagents) to acid chlorides results in ketones. 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