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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568293Generated: October 29, 2026

Thionyl Chloride → HCID 21262359, compound

https://huagongshe.com/reaction/568293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 21262429HCID 21262429—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21262359HCID 21262359—

Reaction Conditions

Temperature85 °C

Reaction Steps

3-Hydroxymethyl-5-methylimidazo[5,1-b]thiazolehydrochloride (1.10 g) is suspended in 20 ml of THF, 0.7 ml of thionyl chloride is added thereto, and the mixture is stirred at 85° C. for 3.5 hr. The solvent is removed by evaporation to give 1.10 g of 3-chloromethyl-5-methylimidazo[5,1-b]thiazolehydrochloride. This compound is dissolved in 7 ml of DMF, 1.36 g of triphenylphosphine is added thereto, and the mixture is stirred at 83° C. for 15 hr and at 90° C. for 4 hr. The resultant precipitate is collected by filtration and washed with diethyl ether to give 1.87 g of (5-methylimidazo[5,1-b]thiazol-3-yl)methyltriphenylphosphonium chloride hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180622B2
Source datasetuspto-grants-2001_01
ORD IDord-dddfb79fd9314c718f0bf68916d15f45
Source noteuspto-grants-2001_01