New downstream synthetic route of 5406-86-0

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 5406-86-0, 2-(4-(tert-Butyl)phenyl)ethanol.

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. 5406-86-0, name is 2-(4-(tert-Butyl)phenyl)ethanol. A new synthetic method of this compound is introduced below., SDS of cas: 5406-86-0

EXAMPLE A STR20 5.4 g (0.03 mol) of 2-(4-tert-butylphenyl)ethanol were added dropwise at 50 C. to a suspension of 1.2 g (0.03 mol) of sodium hydride (60% dispersion in oil) in 50 ml of dry dimethylformamide, and the mixture was stirred until the evolution of hydrogen had ceased. The mixture was cooled to 0 C., and 4.7 g (0.025 mol) of 4-chloro-5-methoxy-6-methoxymethylpyrimidine (Coll. Czechoslov. Chem. Commun. 33, 2266 (1968)) were added. The mixture was stirred for 1 hour at room temperature and for 2 hours at 100 C. After the solvent had been stripped off, the residue was taken up in dichloromethane/water, and the organic phase was dried and evaporated on a rotary evaporator. The crude product was chromatographed on silica gel using ethyl acetate. 3.8 g (46% of theory) of 4-[2-(4-tert-butylphenyl)ethoxy]-5 -methoxy-6 -methoxymethylpyrimidine were obtained in the form of a yellow oil.

If you are interested in these compounds, you can also browse my other articles.Thank you for taking the time to read this article. I hope you enjoyed it, 5406-86-0, 2-(4-(tert-Butyl)phenyl)ethanol.

Reference:
Patent; Hoechst Schering AgrEvo GmbH; US5859020; (1999); A;,
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