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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360965Generated: October 25, 2026

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

https://huagongshe.com/reaction/1360965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,3,3-Trifluoro-2-hydroxypropanoic acidHCID 244896—
ReactantSodium BicarbonateHCID 516892—
Reactant1,2-Diamino-4,5-difluorobenzeneHCID 2736755—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(5,6-Difluoro-1H-benzoimidazol-2-yl-)2,2,2-trifluoro-ethanolHCID 59682276—

Reaction Conditions

Temperature108 °C

Reaction Steps

4,5-Difluoro-benzene-1,2-diamine (4.98 g; 34.5 mmoles) and 3,3,3-trifluoro-2-hydroxy-propionic acid (7.48 g; 51.9 mmoles) were suspended in 6N HCl (8 mL; 48 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 (6.05 g; 72.0 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×40 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 a pale orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879895B2
Source datasetuspto-grants-2011_02
ORD IDord-aa5855963af64ba18324db7efc4be043
Source noteuspto-grants-2011_02