Simple exploration of 6-Chlorohexan-1-ol

At the same time, in my other blogs, there are other synthetic methods of this type of compound,2009-83-8, 6-Chlorohexan-1-ol, and friends who are interested can also refer to it.

Reference of 2009-83-8, Researchers who often do experiments know that organic synthesis is a process of preparing more complex target molecules from simple raw materials through one or more chemical reactions. Generally, it requires fewer steps,and cheap raw materials. 2009-83-8, name is 6-Chlorohexan-1-ol. A new synthetic method of this compound is introduced below.

2.2 Preparation of 6-hydroxyhexyl 3,5-dinitrobenzoate 357.70 g (1.686 MoI) of 3,5-dinitrobenzoic acid are suspended in 750 ml of 1-methyl-2- pyrrolidone. The suspension is stirred up to 500C. 386.36 g (4.599 MoI) of sodium hydrogen carbonate are added and the mixture was heated up to 900C. 22.50 g (0.150 MoI) of sodium iodide and 204.0 ml (1.533 MoI) of 6-chlorohexanol are added to the reaction mixture which is heated to 1000C for 1 h. After 1 h of reaction, the reaction is complete and the orange suspension is thrown on 2 I of ice and1 I of water. The product is filtrated, washed water and dried at 5O0C under vacuum for 24 h to give 425.0 g (91%) of 6-hydroxyhexyl 3,5-dinitrobenzoate as a rose powder.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,2009-83-8, 6-Chlorohexan-1-ol, and friends who are interested can also refer to it.

Reference:
Patent; ROLIC AG; WO2008/145225; (2008); A2;,
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts