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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182357Generated: November 1, 2026

Trifluoroacetic acid → HCID 178466031, compound

https://huagongshe.com/reaction/2182357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178522794HCID 178522794—
ProductHCID 178466031HCID 178466031—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of trifluoroacetic acid (6 mL) and 2-(5-ethoxy-1H-pyrazol-3-yl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-benzoimidazole (300 mg, Reference Example 11) was stirred at 50° C. for 1.5 hours. The reaction mixture was evaporated and the residue was partitioned between ethyl acetate and water (pH 10). The organic layer was dried and then evaporated. The residue was subjected to chromatography on silica eluting with a mixture of dichloromethane and methanol (9:1, v/v) and then recrystallised from toluene to give 2-(5-ethoxy-1H-pyrazol-3-yl)-1H-benzoimidazole (0.1 g) as a colourless solid, mp 217-219.5° C. [Elemental analysis: C, 62.26%; H, 5.23%; N, 23.44%. Calculated for C12H12N4O: C, 63.15%; H, 5.30%; N, 24.55%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897208B2
Source datasetuspto-grants-2005_05
ORD IDord-323c0b5aa1e44caf845fe89561e40b1c
Source noteuspto-grants-2005_05