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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34622생성일: 2026년 10월 24일

Hydrochloric Acid → 4-Chloro-5-(4-chlorophenoxy)-2-nitrobenzoic Acid

https://huagongshe.com/ko/reaction/34622

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-ChlorophenolHCID 4684—
반응물Sodium hydrideHCID 24758—
반응물4,5-Dichloro-2-nitrobenzoic acidHCID 583642—
용매DiglymeHCID 8150—
생성물4-Chloro-5-(4-chlorophenoxy)-2-nitrobenzoic AcidHCID 14233424—

반응 조건

온도10 °C

반응 단계

To 30 ml of dry diglyme under a nitrogen atmosphere was added 0.960 g (0.02 mol) of sodium hydride dispersion in mineral oil (50%). The solution was cooled to 10° C. and 1.28 g (0.01M) 4-chlorophenol in 15 ml of dry diglyme was added dropwise while maintaining the temperature at 10° C. This was followed by the dropwise addition of 2.36 g (0.01 mol) of 4,5-dichloro-2-nitrobenzoic acid in 15 ml of dry diglyme. The reaction mixture was then heated to 153° C. (oil bath) for 1 hour and 45 minutes. The reaction mixture was cooled to room temperature and poured into an ice/water mixture. The pH was then adjusted to 1.5 with 6N hydrochloric acid. The solution was extracted with ethyl acetate, and the organic layer dried over anhydrous magnesium sulfate. The solvent was removed and the crude solid triturated with hexane, followed by recrystallization from carbon tetrachloride to give the title compound: yield 1.65 g (50%) m.p. 160°-162° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762838
출처 데이터셋uspto-grants-1988_08
ORD IDord-bdc1d886ab6648aeafdbf5de8eb2e27a
출처 메모uspto-grants-1988_08