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HRID 38550作成日:2026年10月25日

Hydrochloric Acid → 3-Chloro-5-nitrophenol

https://huagongshe.com/reaction/38550

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzene, 1,3-dichloro-5-nitro-HCID 12064—
反応物Potassium HydroxideHCID 14797—
反応物2-DI-Tert-Butylphosphino-2,4,6-TriisopropylbiphenylHCID 66849835—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
溶媒Water ethylacetateHCID 22728543—
生成物3-Chloro-5-nitrophenolHCID 1067581567.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524722B2
出典データセットuspto-grants-2013_09
ORD IDord-6e688c6bb7214519b4f8e556437cacfe
出典メモuspto-grants-2013_09