HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035291Generated: October 30, 2026
Potassium Carbonate → Methyl 2-(4-benzyl-1-(4-methyl-2-nitrophenyl)piperazin-2-yl)acetate
https://huagongshe.com/reaction/1035291
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluoro-3-nitrotoluene | HCID 136287 | — |
| Reactant | 2-Piperazineacetic acid, 4-(phenylmethyl)-, methyl ester | HCID 15665466 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 2-(4-benzyl-1-(4-methyl-2-nitrophenyl)piperazin-2-yl)acetate | HCID 66769743 | — |
Reaction Steps
To a solution of Example 12C (625 mg, 4.03 mmol) in acetonitrile (5 mL) was added 1-fluoro-4-methyl-2-nitrobenzene (1.00 g, 4.03 mmol) and potassium carbonate (1.11 g, 805 mmol). The reaction was heated in an oil bath at 60° C. overnight. The solution was concentrated onto silica gel and purified via flash chromatography (0-100% ethyl acetate/hexanes) to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 7.55-7.60 (m, 1H), 7.22-7.43 (m, 7H), 3.55-3.65 (m, 1H), 3.41-3.59 (m, 2H), 3.36 (s, 3H), 3.09-3.21 (m, 1H), 2.77-2.88 (m, 1H), 2.22-2.62 (m, 7H); MS (APCI+) m/z 384 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546377B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-5d7c561de0d4476c8eb9c7949a97cb21 |
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| Source note | uspto-grants-2013_10 |
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