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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270716Generated: October 25, 2026

Potassium Carbonate → HCID 18451489, compound

https://huagongshe.com/reaction/1270716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
Reactant(3-Methoxyphenyl)boronic acidHCID 2734370—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 18451489HCID 18451489—

Reaction Conditions

Temperature90 °C

Reaction Steps

2,3,5,6-Tetrafluoro-4-bromoaniline (7.5 g, 30.7 mmol) is dissolved in DME (150 mL) and treated with 3-methoxyphenylboronic acid (4.7 g, 30.7 mmol), a catalytic amount of tetrakistriphenylphosphine palladium(0) (0.70 g, 0.6 mmol) and triphenylphosphine (0.66 g, 2.5 mmol). Potassium carbonate (8.5 μg in 50 mL of water) is added and the reaction mixture stirred and heated to 90° C. for 24 hours. After cooling to room temperature most of the DME is removed by rotary evaporator under high vacuum. The resulting material is partitioned between EtOAc (200 mL) and water (250 mL). The organic layer is washed with brine, dried (Na2SO4) and concentrated by rotary evaporator. The crude reaction product is purified by flash chromatography (9:1 hexanes/EtOAc, then 6:4 hexanes/EtOAC) to give 2,3,5,6-tetrafluoro-4-(3′-methoxyphenyl)aniline (m.p. 94–96° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202364B2
Source datasetuspto-grants-2007_04
ORD IDord-c0a8c1fe4a3c4fe9b0f239282dd887b2
Source noteuspto-grants-2007_04