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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297006Generated: October 30, 2026

4'-Bromoacetanilide → N-Acetyl-4-aminobiphenyl

https://huagongshe.com/reaction/1297006

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-BromoacetanilideHCID 7683—
ReactantPhenylboronic AcidHCID 66827—
ReactantPotassium FluorideHCID 522689—
CatalystBiphenylHCID 7095—
Catalystpalladium(II) acetateHCID 167845—
ProductN-Acetyl-4-aminobiphenylHCID 1999886.2%

Reaction Steps

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-di-tert-butylphosphino)biphenyl (6.0 mg, 0.02 mmol, 2.0 mol %), phenylboronic acid (183 mg, 1.5 mmol), potassium fluoride (174 mg, 3.0 mmol), and 4′-bromoacetanilide (214 mg, 1.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) was added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl bromide had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL), filtered through celite, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 182 mg (86%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247731B2
Source datasetuspto-grants-2007_07
ORD IDord-0395838b2c684f0ca9ba7b02469033c7
Source noteuspto-grants-2007_07