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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230456Generated: October 25, 2026

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

https://huagongshe.com/reaction/230456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,3,3-Trifluoro-2-hydroxypropanoic acidHCID 244896—
ReactantSodium BicarbonateHCID 516892—
Reactant4,5-Dinitrobenzene-1,2-diamineHCID 4441903—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(5,6-Dinitro-1H-benzoimidazol-2-yl-)2,2,2-trifluoro-ethanolHCID 59682279—

Reaction Conditions

Temperature108 °C

Reaction Steps

4,5-Dinitro-benzene-1,2-diamine (2.01 g; 10.2 mmoles) and 3,3,3-trifluoro-2-hydroxy-propionic acid (2.22 g; 15.4 mmoles) were suspended in 6N HCl (5 mL; 30 mmoles) and water (4 mL) 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 (40 mL) and with ethyl acetate (40 mL), then sodium bicarbonate (3.79 g; 45.0 mmoles) was added slowly and in portions to quench the reaction. The aqueous layer was separated and extracted with ethyl acetate (3×30 mL). The extracts were combined, washed with water (30 mL) and brine (40 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 numberUS07566733B2
Source datasetuspto-grants-2009_07
ORD IDord-e688501308e44fe9890b16ced0386b35
Source noteuspto-grants-2009_07