HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092034Generated: November 2, 2026
2,6-Dimethylpiperazine → Ethyl 4-(3,5-dimethylpiperazin-1-yl)benzoate
https://huagongshe.com/reaction/1092034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dimethylpiperazine | HCID 66056 | — |
| Reactant | Benzoic acid, 4-fluoro-, ethyl ester | HCID 67976 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 4-(3,5-dimethylpiperazin-1-yl)benzoate | HCID 18425275 | 76% |
Reaction Steps
2,6-Dimethylpiperazine(3.43 g, 30.00 mmol) was added to ethyl 4-fluorobenzoate (1.101 mL, 7.5 mmol), in DMSO (10 mL) warmed to 120° C. under nitrogen. The resulting solution was stirred at 120° C. for 20 h. The reaction mixture was cooled and the solvent was evaporated. The crude product was purified by silica column chromatography, eluting with 10% methanol in dichloromethane containing 1% 0.880 ammonia. Pure fractions were evaporated to dryness to afford ethyl 4-(3,5-dimethylpiperazin-1-yl)benzoate (1.490 g, 76%) as a colourless solid. 1H NMR (399.9 MHz, CDCl3) δ 1.15 (6H, d), 1.37 (3H, t), 2.39 (1H, d), 2.42 (1H, d), 2.97-3.05 (2H, m), 3.65-3.69 (2H, m), 4.33 (2H, q), 6.84-6.87 (2H, m), 7.90-7.93 (2H, m)—NH not seen. MS: m/z=264 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129391B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-50c3548f516b452dbfbe988084a874c9 |
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| Source note | uspto-grants-2012_03 |
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