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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236882Generated: October 26, 2026

Stannane, trimethylphenyl- → Tert-butyl (2-oxo-1-phenyl-1,2-dihydropyridin-4-ylmethyl)-carbamate

https://huagongshe.com/reaction/2236882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, trimethylphenyl-HCID 123095—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-(Boc-aminomethyl)-1H-pyridin-2-oneHCID 42625676—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (2-oxo-1-phenyl-1,2-dihydropyridin-4-ylmethyl)-carbamateHCID 4262567752%

Reaction Steps

To a solution of tert-butyl (2-oxo-1,2-dihydro-pyridin-4-ylmethyl)-carbamate (0.13 g, 0.58 mmol) in dichloromethane (5 mL) is added trimethylphenylstannane (210 μL, 1.2 mmol), followed successively by copper (II) acetate (0.12 g, 0.64 mmol) and tetra-n-butylammonium fluoride (1.0 M solution in tetrahydrofuran, 1.2 mL). The reaction mixture is stirred for 2 days at room temperature and then is quenched by the addition of methanolic ammonia (2 M, 4 mL). The reaction mixture is concentrated and then purified by flash silica gel chromatography (methanol/chloroform) to give tert-butyl (2-oxo-1-phenyl-1,2-dihydropyridin-4-ylmethyl)-carbamate (88 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-af1c765fea00435385b931462349f356
Source noteuspto-grants-2010_05