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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353974Generated: November 2, 2026

2-Bromotoluene → Biphenyl

https://huagongshe.com/reaction/1353974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromotolueneHCID 7236—
ReactantBoronic AcidHCID 61668—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
ProductBiphenylHCID 7095—

Reaction Steps

Cyclization substrate 5 is synthesized in FIG. 1. The Suzuki reaction is iterated, first by coupling 1,3-dimethoxyphen-2-yl boronic acid with 2-bromotoluene with tetrakis(triphenylphosphine) palladium catalysis to give biphenyl compound 1. Regioselective bromination of 1 gave 2, followed by Suzuki reaction with pyridine-3-boronic acid under palladium catalysis to yield 3. Demethylation of 3 with hydrobromic acid and acetic acid gave 4, followed by Friedel-Crafts acylation with 2,5-dichlorotrimellitic anhydride to yield 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039663E1
Source datasetuspto-grants-2007_05
ORD IDord-f424cb1166df4f0fba75b19f91deb8c4
Source noteuspto-grants-2007_05