Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091946Generated: November 1, 2026

Sodium Carbonate → HCID 68509393, compound

https://huagongshe.com/reaction/2091946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDibutyl Vinylboronate (stabilized with Phenothiazine)HCID 236543—
ReactantHCID 67155404HCID 67155404—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 68509393HCID 68509393—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 5′-chloro-N,2′-dimethyl-4′-nitrobiphenyl-4-carboxamide (Step 2, 100 mg, 0.33 mmol), vinylboronic acid dibutyl ester (90 mg, 0.5 mmol) and sodium carbonate (245 mg, 2.31 mmol) in THF/H2O (8/2 mL) is added dichlorobis(triphenylphospine) palladium (II) (12 mg, 5% mmol). The reaction tube is sealed, the mixture is purged with N2 for 3 min and then heated at 90° C. under N2 for overnight. The reaction is cooled to room temperature and poured into saturated aqueous ammonia chloride solution. The crude reaction mixture is extracted with ethyl acetate (3×15 mL). The organic extracts are combined, washed with brine and concentrated. The crude product is purified with silica gel column chromatography (30% ethyl acetate in DCM) to afford N,2′-dimethyl-4′-nitro-5′-vinylbiphenyl-4-carboxamide as a yellow solid. The obtained solid is dissolved in methanol (20 mL). To this solution is added Pd/C (10%). The reaction mixture is degassed and purged with H2 for several times and stirred under atmospheric hydrogen overnight. The mixture is filtered and concentrated to afford 4′-amino-5′-ethyl-N,2′-dimethylbiphenyl-4-carboxamide as a yellow solid. ESMS m/z 269.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440681B2
Source datasetuspto-grants-2013_05
ORD IDord-7dfd4a31849544bf84bd4db5184320ea
Source noteuspto-grants-2013_05