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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795667Generated: October 31, 2026

Sodium Carbonate → 2-Bromo-4'-(trifluoromethyl)-1,1'-biphenyl

https://huagongshe.com/reaction/1795667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-2-iodobenzeneHCID 11415—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
CatalystHCID 178418397HCID 178418397—
Product2-Bromo-4'-(trifluoromethyl)-1,1'-biphenylHCID 1204072667.1%

Reaction Conditions

Temperature85 °C

Reaction Steps

An oven dried Schlenk tube was evacuated and backfilled with argon and charged with tetrakis(triphenylphosphine)palladium (289 mg, 0.25 mmol, 5.0 mol %), 2-bromoiodobenzene (0.83 mL, 6.50 mmol), 4-(trifluoromethyl)phenylboronic acid (950 mg, 5.0 mmol), and sodium carbonate (2.86 g, 27.0 mmol). The tube was evacuated and backfilled with argon. To the tube was added (degassed) dimethoxyethane (45 mL), ethanol (2 mL), and water (15 mL) through a rubber septum. The reaction mixture was heated to 85° C. with stirring for 32 hours. The reaction mixture was then diluted with 2:1 hexane/ethyl acetate (100 mL) and poured into a separatory funnel. The mixture was washed with water (80 mL), and brine (80 mL). The organic layer was dried over anhydrous sodium sulfate, decanted, and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel to afford 1.01 g (67%) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026498B2
Source datasetuspto-grants-2006_04
ORD IDord-5446a743197447968089ceb12e61abdf
Source noteuspto-grants-2006_04