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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341691Generated: October 30, 2026

Cesium carbonate → (4'-Chloro-3,5-diethylbiphen-4-yl)carbamic acid

https://huagongshe.com/reaction/341691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
Reactanttert-Butyl (4-bromo-2,6-diethylphenyl)carbamateHCID 59450511—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product(4'-Chloro-3,5-diethylbiphen-4-yl)carbamic acidHCID 131732100—

Reaction Steps

A solution of cesium carbonate (89.12 g, 0.27 mol) in water (600 ml) is added to a degassed solution of (4-bromo-2,6-diethylphenyl)carbamic acid tert-butyl ester (30 g, 0.091 mol) and 4-chlorophenylboronic acid (21.54 g, 0.138 mol) in acetone (3000 ml), and the mixture is stirred at room temperature under an atmosphere of nitrogen. Palladium acetate (1.02 g, 0.004 mol) and 2-(dicyclohexylphosphino)-2′,4′,6′-tri-iso-propyl-1,1′-biphenyl (4.33 g, 0.009 mol) are added and the reaction mixture is stirred at room temperature for 12 hours. The mixture is filtered through diatomaceous earth, and the filtrate is evaporated under reduced pressure to remove most of the acetone. The remaining solution is extracted with ethyl acetate (3×300 ml). The organic extracts are combined and concentrated under reduced pressure to give (4′-chloro-3,5-diethylbiphen-4-yl)carbamic acid tent-butyl ester (22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895761B2
Source datasetuspto-grants-2014_11
ORD IDord-c1bb3f67251942fa98fc66ac298dccf8
Source noteuspto-grants-2014_11