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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-chloro-N-methylacetamide | HCID 66773 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Benzyl-piperazin-1-yl)-N-methyl-acetamide | HCID 36845230 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08431695B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-3cf0cccfa4de48788a451027f19e9182 |
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| Source note | uspto-grants-2013_04 |
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