HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760949Generated: October 30, 2026
Sodium Acetate → tert-Butyl 4-(methylamino)piperidine-1-carboxylate
https://huagongshe.com/reaction/1760949
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl 4-(methylamino)piperidine-1-carboxylate | HCID 15380702 | — |
Reaction Steps
Powdered molecular seives (3 Å, 5.2 g), methylamine hydrochloride (16.96 g, 251 mmol), anhydrous sodium acetate (41.21 g, 502 mmol), and 95% sodium cyanoborohydride (3.99 g, 60 mmol) were added sequentially to a solution of 4-oxo-piperidine-1-carboxylic acid tert-butyl ester in methanol (400 mL) at 0° C., and the mixture was allowed to warm to 25° C. over several hours. After 18 hours at 25° C., the reaction mixture was filtered thru Celite®, the solids washed with methanol and ethyl acetate, and the filtrate concentrated. The residue was dissolved in ethyl acetate and the resulting solution washed twice with 2N NaOH, once with brine, dried and concentrated to an oil (12.79 g, 119%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06846820B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-92309b3373064234b5d5443f4787b1b9 |
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| Source note | uspto-grants-2005_01 |
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