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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839311Generated: November 3, 2026

Tributyltin Chloride → HCID 23449202, compound

https://huagongshe.com/reaction/1839311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 23449099HCID 23449099—
ReactantLiHMDS tetrahydrofuranHCID 23714775—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 23449202HCID 23449202—

Reaction Steps

A 1.0 N lithiumbis(trimethylsilyl)amide/THF solution (2.0 ml.) was added to a solution of 0.34 g of 7-trifluoroacetylimidazo[5,1-b]thiazole and 0.48 ml of tri-n-butylstannyl chloride in 16 ml of dry THF in an argon atmosphere at −40° C. The mixture was stirred 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=4:1) to give 0.14 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-f8b8e8f52dc148e1b2025295b4b608e3
Source noteuspto-grants-2004_01