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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38550Generated: October 26, 2026

Hydrochloric Acid → 3-Chloro-5-nitrophenol

https://huagongshe.com/reaction/38550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzene, 1,3-dichloro-5-nitro-HCID 12064—
ReactantPotassium HydroxideHCID 14797—
Reactant2-DI-Tert-Butylphosphino-2,4,6-TriisopropylbiphenylHCID 66849835—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
SolventWater ethylacetateHCID 22728543—
Product3-Chloro-5-nitrophenolHCID 1067581567.8%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524722B2
Source datasetuspto-grants-2013_09
ORD IDord-6e688c6bb7214519b4f8e556437cacfe
Source noteuspto-grants-2013_09