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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38550생성일: 2026년 10월 24일

Hydrochloric Acid → 3-Chloro-5-nitrophenol

https://huagongshe.com/ko/reaction/38550

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzene, 1,3-dichloro-5-nitro-HCID 12064—
반응물Potassium HydroxideHCID 14797—
반응물2-DI-Tert-Butylphosphino-2,4,6-TriisopropylbiphenylHCID 66849835—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
용매Water ethylacetateHCID 22728543—
생성물3-Chloro-5-nitrophenolHCID 1067581567.8%

반응 단계

To a mixture of 1,3-dichloro-5-nitrobenzene (5.00 g, 26.0 mmol), potassium hydroxide (3.44 g, 52.1 mmol), tris(dibenzylideneacetone)dipalladium(0) (539 mg, 0.52 mmol), and 2-(di-tert-butylphosphino)-2,4,6-triisopropylbiphenyl (885 mg, 2.08 mmol) was added a degassed mixture of dioxane (25 mL) and water (15 mL). The mixture was heated for 30 min to 80° C., then diluted with water/ethyl acetate and acidified with diluted hydrochloric acid. The mixture was extracted three times with ethyl acetate. The combined organic layers were dried over sodium sulfate, and the solvent was removed in vacuo. The crude product was purified by column chromatography on silica gel (eluent: cyclohexane/ethyl acetate 3:1). The product was then triturated with petroleum ether/tert-butyl methyl ether and collected by suction filtration to yield 3.06 g (66%) of the title compound as yellowish crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524722B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-6e688c6bb7214519b4f8e556437cacfe
출처 메모uspto-grants-2013_09