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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502996Generated: November 3, 2026

Trifluoroacetic acid → HCID 69377399, compound

https://huagongshe.com/reaction/502996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 131728286HCID 131728286—
SolventChloroformHCID 6212—
ProductHCID 69377399HCID 69377399—

Reaction Steps

Trifluoroacetic acid (2 ml) was added to a chloroform (4 ml) solution of tert-Butyl-{1-[5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-1-methylethyl}carbamate (500 mg), followed by stirring at room temperature for 2 hours. The reaction solution and chloroform were added to an aqueous saturated sodium hydrogen carbonate solution and then the organic layer was separated. Furthermore, the organic layer washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered and then the solvent was removed by evaporation under reduced pressure. Potassium carbonate (394 mg) and 1,2-bis(bromomethyl)benzene (376 mg) were added to a DMF (10 ml) solution of the resulting residue, followed by stirring at 60° C. for 14 hours. Distilled water and chloroform were added to the reaction solution and then the organic layer was separated. Furthermore, the organic layer washed with an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered and then the solvent was removed by evaporation under reduced pressure. The resulting crude product was purified by flash chromatography (chloroform:methanol=25:1) to obtain 35 mg of 2-{1-[5-(2-chlorophenyl)-4-methyl-4H-1,2,4-triazol-3-yl]-1-methylethyl} isoindoline (colorless solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776897B2
Source datasetuspto-grants-2010_08
ORD IDord-cfd7f186d537472f925f9c2b23ffb0c1
Source noteuspto-grants-2010_08