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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244176Generated: October 31, 2026

Potassium Phosphate, Tribasic → (1,1'-Biphenyl)-3-ol, 4-nitro-

https://huagongshe.com/reaction/1244176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPhenyl dihydrogen orthoborateHCID 78412—
Reactant2-(Dicyclohexylphosphino)biphenylHCID 2734216—
Reactant4-Chloro-2-(ethoxymethoxy)-1-nitrobenzeneHCID 12994714—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(1,1'-Biphenyl)-3-ol, 4-nitro-HCID 87437—

Reaction Conditions

Temperature80 °C

Reaction Steps

9.3 g (40 mmol) of 4-chloro-2-(ethoxymethoxy)-1-nitrobenzene from step A and 7.3 g (60 mmol) of phenylboric acid were dissolved in 170 mL of toluene under nitrogen. Then, 0.1 g (0.5 mmol) of palladium acetate, 0.35 g (1 mmol) of 2-(dicyclohexylphosphino)biphenyl and 15 g of tripotassium phosphate were added, and the reaction mixture was heated to 80° C. At the end of the reaction, the reaction mixture was poured into 100 mL of ethyl acetate and the organic phase was extracted with dilute sodium hydroxide solution and then dried over magnesium sulfate. The solvent was distilled off in a rotary evaporator, and the residue was purified on silica gel with hexane/ethyl acetate (9:1). The resulting product dissolved in 50 mL of ethanol was heated to 50° C. 80 mL of a 2.9-molar ethanolic hydrochloric acid solution was then added dropwise after which the reaction mixture was cooled to 0° C. The precipitate was filtered off, washed twice with 20-mL portions of ethanol and then dried. This gave 9.35 g of 4-nitro-1,1′-biphenyl-3-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122061B2
Source datasetuspto-grants-2006_10
ORD IDord-dfa6d512d5ba496cb4854a7d3ae7b3e8
Source noteuspto-grants-2006_10