HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870617Generated: November 1, 2026
Trifluoroacetic acid → HCID 18695982, compound
https://huagongshe.com/reaction/1870617
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-Tert-butoxycarbonyl-4-(5-fluoro-3-(2,2,2-trifluoroethyl)-2-oxo-1-benzimidazolinyl)piperidine | HCID 18695964 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18695982 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06096763 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-e2c2ab1e3a444c6fade92af0dea895ed |
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| Source note | uspto-grants-2000_08 |
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