Adding a certain compound to certain chemical reactions, such as: 2009-83-8, 6-Chlorohexan-1-ol, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, 2009-83-8, blongs to alcohols-buliding-blocks compound. SDS of cas: 2009-83-8
In addition, the mixture was stirred at a stirrer, condenser, and a reaction vessel provided with a thermometer 4-hydroxy-benzoic acid 13.8g (100 mmol), potassium iodide 2.5g, 0.7g tetrabutyl ammonium bromide, and 400ml of ethanol were charged at room temperature.It was added dropwise a 25% aqueous solution of sodium hydroxide, 12g slowly.After the addition, maintaining the reaction vessel at 50 , and was added dropwise to 6-chloro-hexanol 20g (150 mmol) slowly.After the addition was completed, the reaction vessel also by heating to 70 by further reaction for 3 hours.After completion of the reaction, neutralized with 10% hydrochloric acid and subjected to extraction with ethyl acetate, dried over sodium sulfate, the solvent was concentrated to 17g to synthesize compounds shown in formula (23).
These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,2009-83-8, its application will become more common.
Reference:
Patent; DIC Corporation; Hayashi, Masanao; Nagashima, Yutaka; Kusumotto, Tetsuo; (24 pag.)KR101523330; (2015); B1;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts