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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683721Generated: October 31, 2026

Trichloroacetyl chloride → 2,9-Dimethyl-3-trichloroacetylimidazo[1,2-a]benzimidazole

https://huagongshe.com/reaction/1683721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl chlorideHCID 6420—
Reactant2,4-Dimethylimidazo[1,2-a]benzimidazoleHCID 828269—
SolventO-XyleneHCID 7237—
Product2,9-Dimethyl-3-trichloroacetylimidazo[1,2-a]benzimidazoleHCID 19040812—

Reaction Steps

Pour 5.45 g (30 mmol) of freshly distilled trichloroacetyl chloride dropwise into a boiling solution of 2,9-dimethylimidazo[1,2-a]benzimidazole(3.7 g; 20 mmol) obtained as described in Khim. Geterotsikl Soedin, 86, (7), 918-925--in 50 ml of xylene, with vigorous stirring, over a period of 20 to 30 minutes. The mixture is then heated at reflux for wo hours until the product which has initially precipitated is completely dissolved. Cool and filter. Concentrate the mother liquors and add petroleum ehter. Combie with the precipitate obtained earlier and repeat the operation. The combined precipitates are treated with an aqueous solution of sodium hydrogen carbonate and then recrystallised from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639756
Source datasetuspto-grants-1997_06
ORD IDord-771fdf85b83348c9a668a315d8e78fef
Source noteuspto-grants-1997_06