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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1448415생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1448415

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물Diethylene Glycol Monobutyl EtherHCID 8177—
반응물Sodium hydrideHCID 24758—
반응물3,5-Dichloro-2,6-difluoropyridineHCID 643277—
생성물2-[2-(2-Butoxyethoxy)ethoxy]-3,5-dichloro-6-fluoropyridineHCID 20379599—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04180395
출처 데이터셋uspto-grants-1979_12
ORD IDord-a16c58c74aab4c17b8c0556f9628f0e1
출처 메모uspto-grants-1979_12