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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1086021생성일: 2026년 10월 23일

Iodine → 2,4-Dichloro-3-ethyl-6-nitrophenol

https://huagongshe.com/ko/reaction/1086021

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Nitric AcidHCID 944—
반응물4-Ethylbenzenesulfonic acidHCID 7402—
반응물ChlorineHCID 24526—
반응물2,3,5-Trichloro-4-ethylbenzenesulfonic acidHCID 14597440—
용매WaterHCID 962—
용매Sulfuric AcidHCID 1118—
생성물2,4-Dichloro-3-ethyl-6-nitrophenolHCID 7020339—

반응 단계

Iodine (5 parts) was dissolved in 96% sulfuric acid (1000 parts) and 4-ethylbenzenesulfonic acid (186 parts) was added thereto. Chlorine (about 235 parts) was introduced therein, while being stirred at a temperature of 40° to 60° C. Then, a 2,3,5-trichloro-4-ethylbenzenesulfonic acid content in the reaction mixture reached 78.3%. Successively, water (200 parts) was added to the reaction mixture so as to make a ratio of sulfuric acid to water 8:2, and the reaction mixture was subjected to steam distillation at a temperature of 160° to 200° C., thereby performing desulfonation reaction. Mixed acid consisting of 67% nitric acid (110 parts) and concentrated sulfuric acid (174 parts) was added dropwise to the desulfonation reaction product isolated from water, while being stirred at a temperature of 20° to 40° C., and the mixture was kept at that temperature for 1 to 3 hours. Thereafter, the reaction mixture was poured into water (950 parts) at a temperature of 30° C. or below. The reaction product was separated from water and then washed with water. The crude product of 2,3,5-trichloro-4-ethylnitrobenzene (220 parts) was added to a mixture of methanol (1560 parts), water (200 parts) and potassium hydroxide (240 parts), and the resulting mixture was refluxed for 4 hours. Thereafter, the reaction mixture was cooled to ambient temperature to deposit precipitate. The precipitate separated and washed with methanol and then water was placed in 20 % sulfuric acid (510 parts). The mixture was stirred for 3 hours at a temperature of 70° to 75° C., and then cooled to produce crystals of 2,4-dichloro-3-ethyl-6-nitrophenol. The crystals were collected on a filter, washed with water and then dried to obtain a desired product (141.8 parts). The over-all yield from 4-ethylbenzenesulfonic acid was found to be 60.1 %. The product had a melting point of 45.1° to 46.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05012015
출처 데이터셋uspto-grants-1991_04
ORD IDord-ba506011cf844737b47558b264dcf79e
출처 메모uspto-grants-1991_04