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HRID 1448415作成日:2026年10月27日

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

https://huagongshe.com/reaction/1448415

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Diethylene Glycol Monobutyl EtherHCID 8177—
反応物Sodium hydrideHCID 24758—
反応物3,5-Dichloro-2,6-difluoropyridineHCID 643277—
生成物2-[2-(2-Butoxyethoxy)ethoxy]-3,5-dichloro-6-fluoropyridineHCID 20379599—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04180395
出典データセットuspto-grants-1979_12
ORD IDord-a16c58c74aab4c17b8c0556f9628f0e1
出典メモuspto-grants-1979_12