HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643960Generated: November 2, 2026
Sodium Bicarbonate → tert-Butyl 3-(4-benzylpiperazin-1-yl)piperidine-1-carboxylate
https://huagongshe.com/reaction/1643960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N,N-Bis(2-chloroethyl)benzylamine hydrochloride | HCID 2777881 | — |
| Reactant | 3-Aminopiperidine hydrochloride, N1-BOC protected | HCID 17750334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 3-(4-benzylpiperazin-1-yl)piperidine-1-carboxylate | HCID 86642500 | — |
Reaction Steps
4.90 g (21.1 mmol) of benzylbis(2-chloroethyl)amine hydrochloride were dissolved in ethanol (120 ml) and, while stirring, 5.00 g (21.1 mmol) of tert-butyl 3-aminopiperidine-1-carboxylate hydrochloride and 14.2 g (169 mmol) of sodium bicarbonate were added. The resulting reaction solution was heated under reflux for 4 h. The cooled reaction mixture was concentrated in vacuo, 100 ml of water were added, and the aqueous phase was extracted with ethyl acetate (4×60 ml). The combined organic phases were washed with saturated aqueous NaHCO3 solution, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by chromatography on silica gel (mobile phase gradient 0-5% methanol in dichloromethane). Yield: 6.99 g (75%) of yellow solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119676B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-da4c5a17c36e4fcc914bbcd43242ca4a |
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| Source note | uspto-grants-2012_02 |
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