HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063309Generated: October 31, 2026
Ammonium Acetate → Tert-butyl 4-amino-3,3-dimethylpiperidine-1-carboxylate
https://huagongshe.com/reaction/1063309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-Butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate | HCID 22278899 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 4-amino-3,3-dimethylpiperidine-1-carboxylate | HCID 10171391 | — |
Reaction Steps
Ammonium acetate (700 g, 9.09 mol) was added to a stirred solution of 1-t-butyloxy carbonyl-3,3-dimethyl-4-piperidone (352 g, 1.55 mol) in methanol (1.0 L). The suspension was stirred for 3 hr at 20-30° C. The reaction mixture was cooled to 0° C. and sodiumcyanoborohydride (45 g, 0.71 mol) was added portion wise over 30 minutes. Cooling was removed and the suspension was stirred for 12 hr at 20-30° C. The reaction mixture was concentrated to dryness, stirred with water (2.0 L) and extracted with 1.0 L×3 dichloromethane. Combined organic extract was washed with water and dried over sodium sulfate. Evaporation of organic solvent afforded the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06964966B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-e61591f3213a46df8d6f94577f968336 |
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| Source note | uspto-grants-2005_11 |
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