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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798994Generated: October 27, 2026

Toluene → 2'-Chloro-4'-fluoro-biphenyl-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1798994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Bromo-2-chloro-4-fluorobenzeneHCID 2733406—
ReactantEthyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 2773962—
SolventWaterHCID 962—
Product2'-Chloro-4'-fluoro-biphenyl-2-carboxylic acid ethyl esterHCID 59492609125.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a reaction vessel were added 1-bromo-2-chloro-4-fluorobenzene (25 g), ethyl 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (46 g), toluene (125 ml), water (125 ml) and tripotassium phosphate (50.5 g), and purged with argon. To this mixture was added dichlorobis(triphenylphosphine)palladium(II) (1.67 g) and the mixture was stirred in an oil bath at 110° C. for 3 hr. The oil bath was removed, and water (125 ml) was added to the reaction mixture. The mixture was stirred at room temperature for 1 hr, and filtered through celite. The filtrate was partitioned in a separatory funnel. The aqueous layer was extracted with toluene, and the organic layers were combined. The organic layer was washed twice with water (125 ml), dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give the title compound (41.8 g). The obtained solid was directly used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343994B2
Source datasetuspto-grants-2013_01
ORD IDord-20cf5f640dac4fa88fb8546a54b2d7d1
Source noteuspto-grants-2013_01