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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230447Generated: October 25, 2026

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

https://huagongshe.com/reaction/230447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,3,3-Trifluoro-2-hydroxypropanoic acidHCID 244896—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-5-fluoro-1,2-phenylenediamineHCID 735773—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(5-Chloro-6-fluoro-1H-benzoimidazol-2-yl)-2,2,2-trifluoro-ethanolHCID 59682286—

Reaction Conditions

Temperature108 °C

Reaction Steps

4-Chloro-5-fluoro-benzene-1,2-diamine (5.20 g; 32.4 mmoles) and 3,3,3-trifluoro-2-hydroxy-propionic acid (7.00 g; 48.6 mmoles) were suspended in 6N HCl (9 mL; 54 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 (100 mL) and with ethyl acetate (100 mL), then sodium bicarbonate (6.90 g; 81.00 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×40 mL). The extracts were combined, washed with water (30 mL) and brine (30 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 an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566733B2
Source datasetuspto-grants-2009_07
ORD IDord-448d8033955f45bcba9f866c640fede6
Source noteuspto-grants-2009_07