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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607090Generated: October 25, 2026

Potassium Carbonate → Methyl 3'-amino-4'-chloro-2-methylbiphenyl-4-carboxylate

https://huagongshe.com/reaction/607090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-bromo-3-methylbenzoateHCID 3294148—
Reactant3-Amino-4-chlorophenylboronic acidHCID 4341643—
CatalystHCID 178418807HCID 178418807—
SolventAcetoneHCID 180—
ProductMethyl 3'-amino-4'-chloro-2-methylbiphenyl-4-carboxylateHCID 57704763—

Reaction Conditions

Temperature70 °C

Reaction Steps

(3-amino-4-chlorophenyl)boronic acid (1.0 g, 5.834 mmol), methyl 4-bromo-3-methylbenzoate (1.337 g, 5.834 mmol), 1,1′-bis(diphenylphosphino)ferrocene-palladium dichloride dichloromethane adduct (476 mg, 0.583 mmol), aqueous potassium carbonate (11.57 mL, 1M, 11.57 mmol) and acetone (53 mL) were mixed and heated in a 70° C. oil bath for 1.5 hours to complete the coupling. Volatiles were removed from the crude mixture under reduced pressure. The resulting mixture was treated with water followed by ethyl acetate extraction. The combined extracts were dried over Na2SO4, filtrated and concentrated under reduced pressure to afford a dark oil. The resulting oil was purified by flash chromatography (SiO2, Biotage 40+M cartridge, 0-40% EtOAc in hexanes) to afford methyl 3′-amino-4′-chloro-2-methylbiphenyl-4-carboxylate. LCMS calc.=275.07; found=276.23 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915271B2
Source datasetuspto-grants-2011_03
ORD IDord-c13586b29ca64db7a3a29b5626b32e0e
Source noteuspto-grants-2011_03