HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168659Generated: October 30, 2026
Sodium Bicarbonate → HCID 67372299, compound
https://huagongshe.com/reaction/2168659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67387275 | HCID 67387275 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67372299 | HCID 67372299 | — |
Reaction Steps
To a stirred suspension of ethyl 1-benzyl-4-oxo-piperidine-3-carboxylic acid ethyl ester hydrochloride salt (83.95 mmol, 25 g) in EtOAc (400 mL) was added saturated sodium bicarbonate solution (100 mL) and continued stirring for 1 h. The organic layer was separated, dried over, filtered and concentrated to get ethyl 1-benzyl-4-oxo-piperidine-3-carboxylic acid ethyl ester. To a solution of ethyl 1-benzyl-4-oxo-piperidine-3-carboxylic acid ethyl ester in EtOAc (100 mL) was added (Boc)2O (27.48 g) followed by 10% Pd—C (5 g) and the resultant reaction mixture was subjected to hydrogenation at 50 psi of hydrogen for 24 h. The catalyst was filtered by passing through a pad of celite, washed the celite pad with EtOAc (200 mL) and the combined filtrate was concentrated. The residue was purified by flash silica gel column chromatography by eluting with 10% ethyl acetate in hexanes to get ethyl 4-oxo-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (24.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045461B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-d4e5a5c21baf4a9b8a9faa6720cb3a68 |
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| Source note | uspto-grants-2015_06 |
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