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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427507Generated: October 26, 2026

Sodium Carbonate → 4-Bromo-4'-(trifluoromethyl)biphenyl

https://huagongshe.com/reaction/1427507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Catalystpalladium(II) acetateHCID 167845—
Product4-Bromo-4'-(trifluoromethyl)biphenylHCID 1271234970.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A 250 mL flask was charged with 4-(trifluoromethyl)phenylboronic acid (4.85 g, 25.5 mmol), 4-bromoiodobenzene (7.22 g, 25.5 mmol), Pd(OAc)2 (57.2 mg, 0.255 mmol) and sodium carbonate (5.41 g, 51.0 mmol). The flask was flushed with nitrogen, then n-propanol (40 mL) and water (8 mL) were added. The mixture was stirred at 100° C. overnight. The reaction mixture was cooled to room temperature and diluted with water. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The crude residue was purified by silica gel chromatography to provide 4-bromo-4′-(trifluoromethyl)biphenyl (5.4 g, 70%) as a colorless solid. 1H NMR (400 MHz, CDCl3) δ 7.62-7.73 (m, 4H), 7.57-7.61 (m, 2H), 7.43-7.47 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933104B2
Source datasetuspto-grants-2015_01
ORD IDord-fb26d45eb4dd4d37b2a6d79b0db8319d
Source noteuspto-grants-2015_01