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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714263Generated: October 25, 2026

Hydrochloric Acid → 1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanol

https://huagongshe.com/reaction/1714263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4,5-Dichloro-1,2-phenylenediamineHCID 79297—
Reactant3,3,3-Trifluoro-2-hydroxypropanoic acidHCID 244896—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(5,6-dichloro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanolHCID 11637778—

Reaction Conditions

Temperature108 °C

Reaction Steps

4,5-Dichloro-benzene-1,2-diamine (8.50 g; 48.0 mmoles) and 3,3,3-trifluoro-2-hydroxy-propionic acid (10.59 g; 73.52 mmoles) were suspended in 6N HCl (19 mL; 114 mmoles) under a nitrogen atmosphere. The reaction was stirred vigorously and heated to 108° C. for 18 hrs, then cooled to room temperature. The reaction was diluted with water (200 mL) and with ethyl acetate (200 mL), then sodium bicarbonate (6.05 g; 72.0 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×80 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 which was then purified by column chromatography (SiO2; 30% ethyl acetate/CH2Cl2) to yield the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795446B2
Source datasetuspto-grants-2010_09
ORD IDord-eed810adb1294227b4ef751a451b5d08
Source noteuspto-grants-2010_09