Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840429Generated: October 31, 2026

Tributyltin Chloride → HCID 22631454, compound

https://huagongshe.com/reaction/1840429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributyltin ChlorideHCID 15096—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 22631774HCID 22631774—
ReactantLiHMDS tetrahydrofuranHCID 23714775—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22631454HCID 22631454—

Reaction Steps

Tri-n-butylstannyl chloride (1.21 ml) and 9.47 ml of a 1.0 N lithiumbis(trimethylsilyl)amide/THF solution were added to a solution of 1.11 g of 7-[3-(4-nitrobenzyloxycarbonyl)aminopropyl]thioimidazo[5,1-b]thiazole in 28 ml of THF at −45° C. under an argon atmosphere, and the mixture was stirred for one hr. An aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted with ethyl acetate, followed by washing with brine. The organic layer was dried over anhydrous magnesium sulfate. The solvent was then removed by distillation, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to prepare 1.24 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680313B2
Source datasetuspto-grants-2004_01
ORD IDord-f2185ee6752942a8acf3812262fddafc
Source noteuspto-grants-2004_01