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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421772Generated: October 26, 2026

Triethylamine → Methyl 2-cyano-4-biphenylcarboxylate

https://huagongshe.com/reaction/1421772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylboronic AcidHCID 66827—
ReactantMethyl 3-Cyano-4-(trifluoromethylsulfonyloxy)benzoateHCID 53821226—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-cyano-4-biphenylcarboxylateHCID 53846446—

Reaction Conditions

Temperature90 °C

Reaction Steps

3-Cyano-4-(trifluoromethanesulfonyloxy)-benzoic acid methyl ester from step 1 (2.5 g, 8.1 mmol) and phenylboronic acid (2 g, 16.2 mmol) were dissolved in DMF (33 ml) and treated with Et3N (3.1 ml, 17.8 mmol). Argon was bubbled into the solution for 20 min. and then a catalytic amount of PdCl2 (PPh3)2 (285 mg, 0.405 mmol) was added. The reaction mixture was warmed to 90° C. and stirred for 3 hours under argon atmosphere. The reaction was quenched with satd. NaHCO3 (20 mL) and extracted with EtOAc (2×20 mL). The organic layer was dried (MgSO4), filtered, and concentrated. The residue was purified by flash chromatography (10% EtOAc/Hexane) to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06077853
Source datasetuspto-grants-2000_06
ORD IDord-ec050cd7113b42ac94b5bac477453797
Source noteuspto-grants-2000_06