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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631954Generated: October 31, 2026

Trifluoroacetic acid → (6-Iodo-2-oxo-2,3-dihydrobenzimidazol-1-yl)phenylacetic acid

https://huagongshe.com/reaction/1631954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 3-(tert-butoxycarbonylphenylmethyl)-5-iodo-2-oxo-2,3-dihydrobenzimidazole-1-carboxylateHCID 66754745—
SolventDichloromethaneHCID 6344—
Product(6-Iodo-2-oxo-2,3-dihydrobenzimidazol-1-yl)phenylacetic acidHCID 66755373—

Reaction Steps

1.50 g (2.73 mmol) of tert-butyl 3-(tert-butoxycarbonylphenylmethyl)-5-iodo-2-oxo-2,3-dihydrobenzimidazole-1-carboxylate (XIIb) were dissolved in dichloromethane (16 ml) and, while stirring at room temperature, trifluoroacetic acid (10 ml) was added. The reaction solution was stirred for 2 h and then the solvent and excess trifluoroacetic acid were removed in vacuo. The residue was taken up again in toluene, concentrated in vacuo and then dried in vacuo. Yield: 1.10 g (100%) of yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791148B2
Source datasetuspto-grants-2014_07
ORD IDord-8990dfa2a3a443f6a856733fff5b2458
Source noteuspto-grants-2014_07