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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870617Generated: November 1, 2026

Trifluoroacetic acid → HCID 18695982, compound

https://huagongshe.com/reaction/1870617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-Tert-butoxycarbonyl-4-(5-fluoro-3-(2,2,2-trifluoroethyl)-2-oxo-1-benzimidazolinyl)piperidineHCID 18695964—
SolventChloroformHCID 6212—
ProductHCID 18695982HCID 18695982—

Reaction Steps

A solution of 1-tert-butoxycarbonyl-4-(5-fluoro-3-(2,2,2-trifluoroethyl)-2-oxo-1-benzimidazolinyl)piperidine (4.17 g, 10 mmol.) in chloroform (50 mL) containing trifluoroacetic acid (5.5 mL) was stirred at room temp. under an inert atmosphere for 6-12 hours until reaction was complete. The solvent and excess TFA were removed and the residue redissolved in chloroform. This solution was washed with Na2CO3 /NaOH solution. The organic layer was dried (Na2SO4), filtered through a pad of charcoal, and the solvent evaporated to give 4-(5-fluoro-3-(2,2,2-trifluoroethyl)-2-oxo-1-benzimidazolinyl)piperidine as a viscous oil which was used as is. A sample of this material was converted to the HCl salt and after crystallization from methanol gave a white solid, mp: >280° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096763
Source datasetuspto-grants-2000_08
ORD IDord-e2c2ab1e3a444c6fade92af0dea895ed
Source noteuspto-grants-2000_08