{"id":272,"date":"2011-01-24T16:45:00","date_gmt":"2011-01-24T16:45:00","guid":{"rendered":"https:\/\/psiconautica.org\/wordpress\/?p=272"},"modified":"2021-11-26T17:58:14","modified_gmt":"2021-11-26T17:58:14","slug":"synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c","status":"publish","type":"post","link":"https:\/\/psiconautica.org\/wordpress\/quimica-avanzada\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\/","title":{"rendered":"Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C)"},"content":{"rendered":"<hr \/>\n<h2>Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C)<\/h2>\n<hr \/>\n<p>2,5-Dimethoxyphenylethylamine (1.81g, 10 mmol) was dissolved in 20ml glacial acetic acid in a 50ml beaker equipped with magnetic stirring and a thermometer, and placed in an ice-bath. Sulfuryl chloride (2.0g, 1.20ml, 15 mmol) was added dropwise<b>1<\/b> to the solution over 30 minutes, the whole time keeping the temperature of the solution between 15-20\u00b0C<b>2<\/b>. When the addition was finished, the ice-bath was removed, and the solution allowed to warm up to room temperature (25\u00b0C) and stirred for another 90 minutes, the temperature being monitored occasionally so that it didn&#8217;t exceed 30\u00b0C. A too high reaction temperature causes partial dichlorination of the substrate, a temperature of 40\u00b0C during the addition invariably causes side reactions.<\/p>\n<p>When the mixture had reacted for a total of 2 hours, 20ml of dry diethyl ether was added, and the solution stirred at room temperature for another 30 minutes, followed by filtration of the precipitated 4-Chloro-2,5-Dimethoxyphenethylamine Hydrochloride and washing with 15ml of dry ether, and air drying to give 0.54g of a white powder. The mother liquor was diluted with an equal amount of dry ether and allowed to stand overnight in the fridge, giving a second crop of 0.74g 2C-C.HCl. The combined crops weighed 1.28g (51% yield) which were and dissolved in a boiling mixture of 50ml acetonitrile and 5ml methanol, which after cooling somewhat was diluted with 30ml dry ether and placed in the fridge to fully crystallize to give 0.67g (27% yield) of pure 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C) Hydrochloride after filtration, washing with 10ml ether and air drying. The recrystallization was very wasteful, and a different solvent system should have been used. Reference [1] suggests methanol\/ether.<\/p>\n<h4>Notes:<\/h4>\n<ol type=\"1\">\n<li>Sulfuryl Chloride is poisonous, and its vapors dissociate into Cl2 and SO2 gas. Use only in a well ventilated area, and preferably chill the bottle before use, as to minimize evaporation.<\/li>\n<li>If the reaction mixture is chilled too much, the acetic acid will solidify, so try to keep the temperature between 15-20\u00b0C and not below.<\/li>\n<\/ol>\n<p><a name=\"refs\"><\/a><\/p>\n<h3>References<\/h3>\n<p>&nbsp;<\/p>\n<p><b>[1]<\/b> <a href=\"..\/pdf\/2c-c.pdf\">Tetrahedron Letters 42, 3247-3249 (2001)<\/a><\/p>\n<hr \/>\n","protected":false},"excerpt":{"rendered":"<p>Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C) 2,5-Dimethoxyphenylethylamine (1.81g, 10 mmol) was dissolved in 20ml glacial acetic acid in a 50ml beaker equipped with magnetic stirring and a thermometer, and placed in an ice-bath. Sulfuryl chloride (2.0g, 1.20ml, 15 mmol) was added dropwise1 to the solution over 30 minutes, the whole time keeping the temperature of the solution [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":1615,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[24],"tags":[],"class_list":["post-272","post","type-post","status-publish","format-standard","has-post-thumbnail","category-quimica-avanzada"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.8 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C) - Psicon\u00e1utica<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"es_ES\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C) - Psicon\u00e1utica\" \/>\n<meta property=\"og:description\" content=\"Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C) 2,5-Dimethoxyphenylethylamine (1.81g, 10 mmol) was dissolved in 20ml glacial acetic acid in a 50ml beaker equipped with magnetic stirring and a thermometer, and placed in an ice-bath. Sulfuryl chloride (2.0g, 1.20ml, 15 mmol) was added dropwise1 to the solution over 30 minutes, the whole time keeping the temperature of the solution [&hellip;]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/psiconautica.org\/wordpress\/quimica-avanzada\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\/\" \/>\n<meta property=\"og:site_name\" content=\"Psicon\u00e1utica\" \/>\n<meta property=\"article:published_time\" content=\"2011-01-24T16:45:00+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2021-11-26T17:58:14+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/psiconautica.org\/wordpress\/wp-content\/uploads\/2011\/01\/1614x1000-1.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1200\" \/>\n\t<meta property=\"og:image:height\" content=\"800\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Ra\u00fal del Pino\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Escrito por\" \/>\n\t<meta name=\"twitter:data1\" content=\"Ra\u00fal del Pino\" \/>\n\t<meta name=\"twitter:label2\" content=\"Tiempo de lectura\" \/>\n\t<meta name=\"twitter:data2\" content=\"2 minutos\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/quimica-avanzada\\\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/quimica-avanzada\\\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\\\/\"},\"author\":{\"name\":\"Ra\u00fal del Pino\",\"@id\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/#\\\/schema\\\/person\\\/3afbb90b66878c42e9d66e8e261f3d29\"},\"headline\":\"Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C)\",\"datePublished\":\"2011-01-24T16:45:00+00:00\",\"dateModified\":\"2021-11-26T17:58:14+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/quimica-avanzada\\\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\\\/\"},\"wordCount\":338,\"commentCount\":0,\"image\":{\"@id\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/quimica-avanzada\\\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/wp-content\\\/uploads\\\/2011\\\/01\\\/1614x1000-1.jpg\",\"articleSection\":[\"Qu\u00edmica avanzada\"],\"inLanguage\":\"es\",\"potentialAction\":[{\"@type\":\"CommentAction\",\"name\":\"Comment\",\"target\":[\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/quimica-avanzada\\\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\\\/#respond\"]}]},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/quimica-avanzada\\\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\\\/\",\"url\":\"https:\\\/\\\/psiconautica.org\\\/wordpress\\\/quimica-avanzada\\\/synthesis-of-4-chloro-25-dimethoxyphenethylamine-2c-c\\\/\",\"name\":\"Synthesis of 4-Chloro-2,5-Dimethoxyphenethylamine (2C-C) - 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