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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230459Generated: October 30, 2026

Hydrochloric Acid → 5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazole

https://huagongshe.com/reaction/230459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4,5-Dichloro-1,2-phenylenediamineHCID 79297—
ReactantSodium BicarbonateHCID 516892—
Reactant3,3,3-Trifluoropropionic acidHCID 2777972—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazoleHCID 11651910—

Reaction Conditions

Temperature108 °C

Reaction Steps

4,5-Dichloro-benzene-1,2-diamine (10.0114 g; 56.5520 mmoles) and 3,3,3-trifluoro-propionic acid (7.5 mL; 84.9 mmoles) were combined with 6N HCl (20 mL; 120 mmoles) and heated to 108° C. for 18 hrs. The reaction mixture was cooled to room temperature, diluted with ethyl acetate (200 mL) and water (200 mL), then then sodium bicarbonate (15.15 g; 180.3 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×60 mL). The extracts were combined, washed with water (60 mL) and brine (60 mL), then dried over Na2SO4. The filtrate was concentrated in vacuo to yield a crude brown solid. A sample of the crude brown solid was purified by column chromatography (SiO2; 100% CH2Cl2) to yield the title compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566733B2
Source datasetuspto-grants-2009_07
ORD IDord-fec8dcb94ff9467b9c2b05f052260e9b
Source noteuspto-grants-2009_07