HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880338Generated: October 26, 2026
Hydrochloride methanol → 1-Acetyl-4-aminopiperidine hydrochloride
https://huagongshe.com/reaction/880338
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | tert-Butyl (1-acetylpiperidin-4-yl)carbamate | HCID 22741830 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Acetyl-4-aminopiperidine hydrochloride | HCID 17221642 | — |
Reaction Steps
To a solution of tert-butyl (1-acetylpiperidin-4-yl)carbamate (330 g, 1.36 mol) in MeOH (1000 mL) was added HCl/MeOH (4M, 300 mL) over 30 min to maintain the temperature at 0° C. After addition, the mixture was stirred at 0° C. for another 2 h and then concentrated to give the crude product. Two batches were run in parallel and produced a combined crude product weight of 310 g. This crude was used in next step without further purification. 1H NMR (400 MHz, D2O) δ 4.35 (dd, J=2.0, 12.0 Hz, 1H), 3.98-3.85 (m, 1H), 3.44-3.30 (m, 1H), 3.18-3.05 (m, 1H), 2.75-2.58 (m, 1H), 2.06-1.92 (m, 5H), 1.61-1.31 (m, 2H); LCMS (m/z): 143.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993555B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-318637a102354fdf82922aae9d9ba85c |
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| Source note | uspto-grants-2015_03 |
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