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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658262Generated: October 26, 2026

Sulfuric Acid → 5-(m-chlorophenyl)-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole hydrochloride

https://huagongshe.com/reaction/1658262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactantm-Chloro-alpha-(2-imidazolin-2-ylaminomethyl)benzyl alcoholHCID 54186887—
Product5-(m-chlorophenyl)-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole hydrochlorideHCID 21510140—

Reaction Steps

4 parts of m-chloro-α-(2-imidazolin-2-ylaminomethyl)benzyl alcohol are added portionwise to 20 parts of cooled (ice-bath) sulfuric acid solution 80%. Upon completion, the whole is stirred for 2 hours at room temperature. The reaction mixture is poured onto crushed ice and the whole is filtered over diatomaceous silica. The filtrate is alkalized with ammonium hydroxide solution at room temperature (cooling is necessary) and the product in base form is extracted with chloroform. The latter is dried and evaporated. The residue is converted into the hydrochloride salt in 2-propanol, yielding 5-(m-chlorophenyl)-2,3,5,6-tetrahydro-1H-imidazo[1,2-a]imidazole hydrochloride; m.p. 249.8°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03963718
Source datasetuspto-grants-1976_06
ORD IDord-276882242893435187dc3e52d8487aaf
Source noteuspto-grants-1976_06