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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178041Generated: October 31, 2026

2-(Trifluoromethyl)benzoic acid → HCID 44203151, compound

https://huagongshe.com/reaction/1178041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethyl)benzoic acidHCID 9899—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 44203151HCID 4420315139%

Reaction Steps

DIPEA (5.7 g, 44.30 mmol) was added drop wise to 2-trifluoromethyl benzoic acid (3.36 g, 17.72 mmol) in DMF (25 mL). EDCI (7.07 gm, 36.91 mmol) and HOBT (2.39 g, 17.72 mmol) were added consecutively and, after 15 minutes, N-Boc piperazine (2.75 g, 14.77 mmoles). The resulting mixture was stirred at room temperature overnight. Water was then added, and the product was extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4 and concentrated under reduced pressure to afford the crude product. Purification using column chromatography (silica gel of mesh size of 60-120 using 30:70 EtOAc:hexane as eluent) afforded 4-(2-trifluoromethyl-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester in 39% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-8e688b55f6074dfc99c1105a2219fc86
Source noteuspto-grants-2010_11