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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359285Generated: October 31, 2026

Pyridazine → 4-(Tributylstannyl)pyrimidine

https://huagongshe.com/reaction/1359285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridazineHCID 9259—
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

58.0 ml of a hexane solution containing 2.52 mol of n-butyllithium was slowly added dropwise into a solution of 200 ml of tetrahydrofuran containing 25.0 mol of 2,2,6,6-tetramethylpiperidine at −30° C. After stirring at 0° C. for 30 minutes, a mixture of 9.1 ml of pyridazine, 46.0 ml of tri-n-butyltin chloride and 100 ml of tetrahydrofuran was slowly added dropwise thereinto at −78° C. 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 NH-silica gel (Fuji Silicia) column chromatography and eluted with hexane/ethyl acetate (10:1). Then, it was subjected to silica gel chromatography and eluted with hexane/ethyl acetate (10:1) and then with hexane/ethyl acetate (1:1), to give 6.6 g of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599917B1
Source datasetuspto-grants-2003_07
ORD IDord-b20b76820cb44d158fe2ed2d4de81a7f
Source noteuspto-grants-2003_07