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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665663Generated: October 26, 2026

3-Fluorobenzoic Acid → 4-(3-Fluoro-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1665663

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluorobenzoic AcidHCID 9968—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(3-Fluoro-benzoyl)-piperazine-1-carboxylic acid tert-butyl esterHCID 57875809107.5%

Reaction Steps

HOBt (290 mg, 2.14 mmol), DIEA (461 mg, 3.5 mmol), EDCI.HCl (410 mg, 2.14 mmol) followed by piperazine-1-carboxylic acid tert-butyl ester (398 mg, 2.14 mmol) were added to a stirred solution of 3-fluorobenzoic acid (250 mg, 1.78 mmol) in DMF (3 mL). The reaction mixture was stirred overnight and then diluted with cold water. The product was extracted with ethyl acetate and the organic layer was washed with brine solution, dried over Na2SO4, and concentrated under reduced pressure to afford 590 mg (92%) of 4-(3-fluoro-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039463B2
Source datasetuspto-grants-2011_10
ORD IDord-68db923e4e6b4683a2dfaab4c13215a0
Source noteuspto-grants-2011_10