HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656602Generated: October 27, 2026
Acetic Acid → 1-Acetyl-4-[2-(6-methyl-2-pyridyl)ethyl]piperazine
https://huagongshe.com/reaction/1656602
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Ethenyl-6-methylpyridine | HCID 70735 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Acetyl-4-[2-(6-methyl-2-pyridyl)ethyl]piperazine | HCID 19788731 | 73% |
Reaction Steps
To a stirring solution of N-acetylpiperazine (2.50 g, 20 mmol) in methanol (40 mL) at 0° C. under nitrogen was added 2-methyl-6-vinyl-pyridine (2.39 g, 20 mmol) and acetic acid (1.28 mL). The mixture was stirred for 24 hours at 80° C. and was then concentrated. The residue was partitioned between 10% aqueous K2CO3 /CH2Cl2. The organic phase was dried and concentrated to afford 3.60 g (73%) of 1-acetyl-4-[2-(6-methyl-2-pyridyl)ethyl]piperazine as a brown solid which was used directly in the next step: 1H NMR (CDCl3): δ 7.48 (m, 1H), 7.0 (d, 1H), 3.63 (t, 2H), 3.45 (t, 2H), 2.95-2.60 (m, 4H), 2.50 (m, s, 9H), 2.08 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05254689 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-f3708cfd7f2443a68628cfa899aa8dbe |
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| Source note | uspto-grants-1993_10 |
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