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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413620Generated: October 26, 2026

Trisodium phosphate dodecahydrate → 4'-n-Propyl-3,5-difluoro-biphenyl-4-ylamine

https://huagongshe.com/reaction/413620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrisodium phosphate dodecahydrateHCID 61473—
Reactant4-Bromo-2,6-difluoroanilineHCID 610191—
Reactant(4-Propylphenyl)boronic acidHCID 4100861—
CatalystBis(triphenylphosphine)palladiumHCID 10122028—
SolventWaterHCID 962—
Product4'-n-Propyl-3,5-difluoro-biphenyl-4-ylamineHCID 7000995699.5%

Reaction Steps

348 g trisodiumphosphate dodecahydrate (Merck KGaA, Art. No.106 578) were dissolved in 500 ml of distilled water. Then 8.563 g bis(triphenylphosphine) palladium (Merck KGaA, Art. No. 804 174) and 0.611 g hydaziniumhydroxide (Merck KGaA, Art. No. 804 604) were added. The suspension was stirred for 5 minutes. Then, 126.886 g 4-bromo-2,6-difluoro-aniline, prepared in house, were added. Next 100 g of the p-n-propylphenyl boronic acid, prepared as described above, dissolved in 600 ml dried tetrahydrafurane (Merck KGaA, Art. No.108 107) was added dropwise. The reaction mixture was heated 6 hours under reflux. The organic layer was separated, dried over Na2SO4 and it's solvent evaporated. The isolated crude product (150 g of 4′-n-propyl-3,5-difluoro-biphenyl-4-ylamine was used for the next step of the reaction without further purificatoin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06569505B2
Source datasetuspto-grants-2003_05
ORD IDord-4abd16b979e747879e943d62a7d5e4d7
Source noteuspto-grants-2003_05