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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972726Generated: November 2, 2026

Ethyl Acetate → 2-(4-Benzyl-piperazin-1-yl)-N-methyl-acetamide

https://huagongshe.com/reaction/1972726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2-chloro-N-methylacetamideHCID 66773—
Reactant1-BenzylpiperazineHCID 75994—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Benzyl-piperazin-1-yl)-N-methyl-acetamideHCID 3684523083%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-benzyl-piperazine (1.0 g, 5.67 mmol), 2-chloro-N-methylacetamide (671.2 mg, 6.24 mmol, 1.1 eq.), and potassium carbonate (941 mg, 6.81 mmol, 1.2 eq.) in anhydrous THF (23 mL) was stirred at 60° C. under N2 for 18 h. The mixture was cooled to rt and poured into EtOAc. The organic phase was washed with water and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by MPLC (Biotage®, gradient elution 1:4:5 v/v MeOH:Acetone:DCM) to give 1.16 g (83%) of the product as a white solid. 1H-NMR (300 MHz, DMSO-d6) 7.62 to 7.56 (broad d, 1H), 7.33 to 7.20 (m, 5H), 3.45 (s, 2H), 2.85 (s, 2H), 2.58 (d, 3H), 2.44 to 2.33 (broad s, 8H); ES-MS m/z 248.2 [M+H]+, RT (min) 0.33.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-3cf0cccfa4de48788a451027f19e9182
Source noteuspto-grants-2013_04