Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656854Generated: November 4, 2026

Fluorobenzene → 4-Bromo-2-fluoro-1,1'-biphenyl

https://huagongshe.com/reaction/1656854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluorobenzeneHCID 10008—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Bromo-2-fluoro-1-iodobenzeneHCID 2724516—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-Bromo-2-fluoro-1,1'-biphenylHCID 52106310%

Reaction Steps

Using methodology generally similar to the above examples, 1.22 g of phenylboronic acid in about 5 ml of ethanol, 3 g of 2-fluoro-4-bromoiodobenzene, 20 g of fluorobenzene, 0.2 g of 5% Pd on carbon catalyst, and 10 ml of 2 molar Na2CO3 were combined and stirred rapidly (without a nitrogen purge) at 25° C. for 65 hours. The desired 2-fluoro-4-bromobiphenyl was produced in about 10% yield with only partial conversion of the starting materials, considerable byproduct formation, but no observed terphenyl formation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05254776
Source datasetuspto-grants-1993_10
ORD IDord-7d0e5e7273064dd2a4ce390c8198263c
Source noteuspto-grants-1993_10