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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663240Generated: October 28, 2026

Diglyme → 4'-Fluoro(1,1'-biphenyl)-2-amine

https://huagongshe.com/reaction/1663240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiglymeHCID 8150—
ReactantSodium CarbonateHCID 10340—
Reactant2-BromoanilineHCID 11992—
ReactantBoronic AcidHCID 61668—
Reactant4-Fluorophenylboronic acidHCID 285645—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product4'-Fluoro(1,1'-biphenyl)-2-amineHCID 2758975—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 2-bromoaniline (1.72 g, 10.0 mmol) in diglyme (30 mL) tetrakis(triphenylphosphine)-palladium(0) (0.13 g, 0.3 mmol) and 2.0 M aqueous sodium carbonate solution (15 mL, 30.0 mmol) were added. In a separate flask, 4-fluorophenylboronic acid (2.23 g 16.0 mmol) was dissolved in ethanol (8 mL) and the mixture containing 2-bromoaniline was added to this boronic acid solution. The obtained brown reaction mixture was heated at 80° C. for 6 hours, then cooled, diluted with ethyl acetate and washed with saturated ammonium chloride solution. The organic layer was dried over sodium sulfate, filtered and concentrated. The residue was purified by flash column chromatography using Kieselgel 60 (0.015-0.040 mm) as adsorbent (Merck) and n-hexane:ethyl-acetate=2:1 as eluent to yield after recrystallization from ethanol 1.8 g (60%) of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034827B2
Source datasetuspto-grants-2011_10
ORD IDord-bde24fca292d47739a7e6cad5611ac38
Source noteuspto-grants-2011_10