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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423314Generated: October 26, 2026

Potassium Carbonate → Methyl 2-cyano-4-biphenylcarboxylate

https://huagongshe.com/reaction/423314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 3-Cyano-4-(trifluoromethylsulfonyloxy)benzoateHCID 53821226—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-cyano-4-biphenylcarboxylateHCID 5384644681.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

The following reaction was split into two batches with half the amounts: methyl 3-cyano-4-{[(trifluoromethyl)sulfonyl]oxy}benzoate (D25) (1.5 g, 4.85 mmol), phenylboronic acid (1.183 g, 9.70 mmol), potassium carbonate (2.011 g, 14.55 mmol) and palladium tetrakistriphenylphosphine(0) (0.561 g, 0.485 mmol) were taken up in DMF (24 ml) and the mixture heated in the microwave for 30 min at 150° C. The two reactions were combined and diluted with ethyl acetate (50 mL) and the mixture filtered through kieselguhr to remove palladium residues. The filtrate was concentrated in vacuo to reduce the amount of DMF and then the residue partitioned between saturated aqueous sodium bicarbonate (50 mL) and ethyl acetate (50 mL). The organic phase was washed with further sodium bicarbonate (50 mL) and then water (50 mL) before it was dried (MgSO4), filtered and the solvent removed in vacuo. The brown solid was purified by silica chromatography, eluting 0-25% EtOAc in iso-hexane over 35 minutes to give the title compound as a white solid (935 mg, 3.94 mmol). δH (d6-DMSO, 400 MHz): 8.42 (1H, d), 8.29 (1H, dd), 7.81 (1H, d), 7.65 (2H, m), 7.60-7.50 (3H, m), 3.92 (3H, s). MS (ES): no mass ion observed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101775B2
Source datasetuspto-grants-2012_01
ORD IDord-8106420cf5ee4036815145707a5a3cc9
Source noteuspto-grants-2012_01