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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356987Generated: October 31, 2026

Trifluoroacetic acid → 4-[4-(4,5-Dihydrooxazol-2-yl)phenyl]piperazine

https://huagongshe.com/reaction/1356987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantn-Tert-butoxycarbonyl-4-[4-(4,5-dihydrooxazol-2-yl)phenyl]piperazineHCID 18504842—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
Product4-[4-(4,5-Dihydrooxazol-2-yl)phenyl]piperazineHCID 18504834—

Reaction Steps

Compound 5A (826 mg; 2.49 mmol) in solution in toluene (20 ml) is treated, at room temperature, with trifluoroacetic acid (2.75 ml). After 1 h, the medium is evaporated to dryness and coevaporated 3 times with toluene. The product obtained is taken up in methanol (20 ml) and triethylamine (8 ml), stirred for 15 min at room temperature and finally evaporated to dryness. The solid obtained is purified by chromatography on a silica gel column eluted with a dichloromethane/methanol/ammonium hydroxide mixture in the proportions 90/9/1 to give the intermediate 5B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589953B2
Source datasetuspto-grants-2003_07
ORD IDord-dc186d8131a54ae5bb8c066db14ae435
Source noteuspto-grants-2003_07