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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157162Generated: November 1, 2026

Trifluoroacetic acid → Methyl 3-(piperazin-1-yl)benzoate

https://huagongshe.com/reaction/1157162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 3-bromobenzoateHCID 12070—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantSodium t-butoxideHCID 23676156—
SolventTolueneHCID 1140—
ProductMethyl 3-(piperazin-1-yl)benzoateHCID 1893072752.5%

Reaction Steps

To a mixture containing piperazine-1-carboxylic acid tert-butyl ester (400 mg, 2.16 mmol), 3-bromo-benzoic acid methyl ester (547 mg, 2.56 mmol), Pd(AcO) (32 mg, 0.14 mmol), 2-(di-t-butylphosphino)biphenyl (80 mg, 0.28 mmol) and sodium t-butoxide (400 mg, 4 mmol) in toluene (20 mL) was degassed with Ar. The reaction mixture was heated at 50 C for overnight. At the end of reaction, ethyl acetate was added and the mixture was filter through celite. After removal of solvent, TFA was added to the residue. The reaction mixture was stirred at ambient temperature for 1 hour. The excess TFA was removed under vacuum and the residue was purified using prep-HPLC to give desired product (250 mg, 37% yield for two steps) as TFA salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807672B2
Source datasetuspto-grants-2010_10
ORD IDord-c0c3a34054e14a23b21b3756a377dcd7
Source noteuspto-grants-2010_10