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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245475Generated: October 30, 2026

Sodium Carbonate → Carbamic acid, (4-(4-formylphenyl)-2-pyridinyl)-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/1245475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Formylphenylboronic AcidHCID 591073—
Reactant(4-Iodo-Pyridin-2-Yl)-Carbamic Acid Tert-Butyl EsterHCID 11484026—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductCarbamic acid, (4-(4-formylphenyl)-2-pyridinyl)-, 1,1-dimethylethyl esterHCID 21912851—

Reaction Steps

Tetrakis(triphenylphosphine)palladium(0) (90 mg, 0.08 mmol, 0.05 equiv) was added to a deoxygenated mixture of tert-butyl 4-iodopyridin-2-ylcarbamate (1-1, 0.500 g, 1.56 mmol, 1 equiv), 4-formylphenyl boronic acid (351 mg, 2.34 mmol, 1.50 equiv), and aqueous saturated sodium carbonate solution (2.0 M, 2.3 mL, 4.7 mmol, 3.0 equiv) in dioxane (15 mL), and the resulting mixture was heated at reflux for 18 h. The reaction mixture was cooled then concentrated. The residue was partitioned between half-saturated aqueous NaCl solution (100 mL) and EtOAc (100 mL). The organic layer was dried over sodium sulfate, and concentrated to give tert-butyl 4-(4-formylphenyl)pyridin-2-ylcarbamate (2-1) as an off-white solid. LRMS m/z (M+H) Calcd: 242.2 (minus t-Bu), 199.2 (minus Boc); found 243.0 and 199.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125888B2
Source datasetuspto-grants-2006_10
ORD IDord-6745573145bb4ac7be1e9bf674f2a298
Source noteuspto-grants-2006_10