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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635358Generated: October 29, 2026

Ethanol → HCID 21258397, compound

https://huagongshe.com/reaction/635358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthylenethioureaHCID 2723650—
ReactantHCID 21258374HCID 21258374—
SolventAcetic AcidHCID 176—
ProductHCID 21258397HCID 21258397—

Reaction Steps

A mixture of the crude 2-bromo-1-[1-(3,4-dichlorophenyl)cyclobutyl]-4-methoxybutan-1-one described above, imidazolidine-2-thione (0.68 g), ethanol (15 ml) and acetic acid (10 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The solvents were removed in vacua and the residue was dried by azeotropic distillation with ethanol (50 ml) followed by ethyl acetate (20 ml). The solid remaining after removal of residual solvent in vacuo was crystallised from a 2:1 mixture of ethanol and ethyl acetate. The resulting product was collected by filtration, washed with ethanol (10 ml) and dried in vacuo at 60°0 C. to give 3-[1-(3,4-dichlorophenyl)cyclobutyl]-2-(2-methoxyethyl)-5,6-dihydroimidazo[2,1-b]-thiazole hydrobromide as colourless prisms (1.39 g), m.p. 227-229° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187802B1
Source datasetuspto-grants-2001_02
ORD IDord-16fa286acdba4551bc6c6c3bff143706
Source noteuspto-grants-2001_02