HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650968Generated: October 27, 2026
Triethylamine → 1-Benzyloxycarbonyl-3-piperidone
https://huagongshe.com/reaction/650968
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Piperidin-3-one | HCID 33722 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Benzyloxycarbonyl-3-piperidone | HCID 1514169 | — |
Reaction Steps
To a solution of 3-piperidone (12 mmol) in 200 mL of methylene chloride. is added triethylamine (18 mmol) in a single portion at room temperature and the reaction mixture cooled to 0° C. Benzyl chloroformate (12 mmol) is added dropwise via addition funnel and the reaction mixture allowed to warm to room temperature. Stirring is continued for 2 hours at room temperature. The reaction mixture is diluted with ethyl acetate (200 mL) and washed with 1N hydrochloric acid (3×100 mL), water and brine. The organic layer is worked up to provide N-Benzyloxycarbonyl-3-piperidone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06277865B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-b80596e8795847d2a8083ccfffd02bdf |
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| Source note | uspto-grants-2001_08 |
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