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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989826Generated: October 30, 2026

Tributyltin Chloride → HCID 23449330, compound

https://huagongshe.com/reaction/989826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 23449178HCID 23449178—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 23449330HCID 23449330—

Reaction Steps

A 1.6 N n-butyllithium/n-hexane solution (1.6 ml ) was added to a solution of 0.26 g of 7-(N-methylsulfamoyl)imidazo[5,1-b]thiazole in 8 ml of dry THF and 4 ml of HMPA in an argon atmosphere at −50° C. The mixture was stirred at the same temperature for 30 min. Tri-n-butylstannyl chloride (0.34 ml) was added thereto. The mixture was stirred for 30 min. A 1.6 N n-butyllithium/n-hexane solution (0.8 ml) was further added thereto. The mixture was stirred for 30 min. Tri-n-butylstannyl chloride (0.2 ml) was added thereto, followed by stirring at the same temperature for 30 min. A saturated aqueous ammonium chloride solution was added thereto. Ethyl acetate was then added, followed by washing with water and saturated brine in that order. The organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:2) to give 0.39 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458780B1
Source datasetuspto-grants-2002_10
ORD IDord-fe26900f761147f595aa360532e210e6
Source noteuspto-grants-2002_10