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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534970Generated: October 31, 2026

Trifluoroacetic acid → 3-(4-{[4-(2-tert-Butylphenyl)piperazin-1-yl]carbonyl}-1,3-oxazol-5-yl)propanoic acid

https://huagongshe.com/reaction/534970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 3-(4-{[4-(2-tert-butylphenyl)piperazin-1-yl]carbonyl}-1,3-oxazol-5-yl)propanoateHCID 66792852—
Product3-(4-{[4-(2-tert-Butylphenyl)piperazin-1-yl]carbonyl}-1,3-oxazol-5-yl)propanoic acidHCID 6679278576.3%

Reaction Steps

A mixture of tert-butyl 3-(4-{[4-(2-tert-butylphenyl)piperazin-1-yl]carbonyl}-1,3-oxazol-5-yl)propanoate (Example 177, 0.60 g, 1.36 mmol) and trifluoroacetic acid (5.0 mL) was stirred at room temperature for 1 h. The reaction mixture was concentrated under reduced pressure and the resulting residue was suspended in water. The mixture was adjusted to pH 4 with 10% NaHCO3 and then extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting white solid was triturated with hexane and ethyl acetate successively to give the title compound (0.40 g) as a white solid: mp 180-181° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-4cc5ed2467244b1696fcb603cfca9174
Source noteuspto-grants-2014_10