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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359283Generated: November 1, 2026

Pyrimidine → 4-(Tributylstannyl)pyrimidine

https://huagongshe.com/reaction/1359283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrimidineHCID 9260—
Reactant2,2,6,6-TetramethylpiperidineHCID 13035—
ReactantTributyltin ChlorideHCID 15096—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(Tributylstannyl)pyrimidineHCID 17830060—

Reaction Conditions

Temperature0 °C

Reaction Steps

5.8 ml of a hexane solution containing 2.52 mol of n-butyllithium was slowly added dropwise into a solution of 20 ml of tetrahydrofuran containing 2.5 ml of 2,2,6,6-tetramethylpiperidine. After stirring at 0° C. for 30 minutes, a mixture of 0.98 ml of pyrimidine, 4.6 ml of tri-n-butyltin chloride and 20 ml of tetrahydrofuran was slowly added dropwise thereinto. After stirring at −78° C. for 4 hours, water was added to the reaction solution and then extracted with ethyl acetate. The organic phase was washed with brine and the solvent was removed. Then, the residue was subjected to silica gel column chromatography to elute with hexane/ethyl acetate (10:1), to give 474 mg of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599917B1
Source datasetuspto-grants-2003_07
ORD IDord-8546d8822e6c42818a7233f527c31070
Source noteuspto-grants-2003_07