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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245470Generated: November 1, 2026

Sodium Carbonate → Tert-butyl 4-phenylpyridin-2-ylcarbamate

https://huagongshe.com/reaction/1245470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant(4-Iodo-Pyridin-2-Yl)-Carbamic Acid Tert-Butyl EsterHCID 11484026—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 4-phenylpyridin-2-ylcarbamateHCID 21912853—

Reaction Steps

Tetrakis(triphenylphosphine)palladium(0) (340 mg, 0.29 mmol, 0.050 equiv) was added to a deoxygenated mixture of tert-butyl 4-iodopyridin-2-ylcarbamate (1-1, 1.87 g, 5.84 mmol, 1 equiv), phenyl boronic acid (1.07 g, 8.76 mmol, 1.50 equiv), and aqueous saturated sodium carbonate solution (2.0 M, 8.8 mL, 18 mmol, 3.0 equiv) in dioxane (50 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. The residue was purified by flash column chromatography (dichloromethane, initially, grading to 40% EtOAc in dichloromethane) to give tert-butyl 4-phenylpyridin-2-ylcarbamate (1-2) as an off-white solid. LRMS m/z (M+H) Calcd: 214.3 (minus t-Bu), 171.3 (minus Boc); found 215.0 and 171.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125888B2
Source datasetuspto-grants-2006_10
ORD IDord-11134824e475461eb96b5610241e6401
Source noteuspto-grants-2006_10