Hexane → 2-[2-(2-Butoxyethoxy)ethoxy]-3,5-dichloro-6-fluoropyridine

A mixture was prepared by admixing 12.9 grams (0.07 mole) of 3,5-dichloro-2,6-difluoropyridine, 100 milliliters of diethyleneglycol n-butyl ether and 3.3 grams (0.75 mole) of a hexane slurry of sodium hydride. The sodium hydride was a 53 percent oil dispersion and had been washed 3 times with 10 milliliter portions of hexane. Considerable foaming occurred and after foaming ceased, the reaction mixture was stirred for ~10 minutes at room temperature and thereafter diluted with 200 milliliters of water. The mixture was extracted 3 times with 100 milliliter portions of hexane, the extracts combined and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The oil which remained as a residue was vacuum distilled to yield 14.3 grams of 2-[2-(2-butoxyethoxy)ethoxy]-3,5-dichloro-6-fluoropyridine as a water-white product. The product had a boiling point of 113°-124° C. at 0.3 millimeters of mercury (mm). Upon analysis, the product was found to have carbon, hydrogen and nitrogen contents of 47.55, 5.37 and 4.36 percent, respectively, as compared with the theoretical contents of 47.87, 5.56 and 4.29 percent, respectively, as calculated for the above named compound.

1. customA mixture was prepared
2. washhad been washed 3 times with 10 milliliter portions of hexane
3. additiondiluted with 200 milliliters of water
4. extractionThe mixture was extracted 3 times with 100 milliliter portions of hexane
5. dry with materialdried over anhydrous sodium sulfate
6. filtrationfiltered
7. concentrationconcentrated under reduced pressure
8. distillationdistilled

ORD-Eintrag

ord-a16c58c74aab4c17b8c0556f9628f0e1

Quelldatensatz

uspto-grants-1979_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04180395