HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095686Generated: October 26, 2026
Sodium Bicarbonate → Naphthalen-2-ylmethyl 3-fluoro-4-oxopiperidine-1-carboxylate
https://huagongshe.com/reaction/1095686
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (Naphthalen-2-yl)methyl carbonochloridate | HCID 15764399 | — |
| Reactant | 3-Fluoropiperidin-4-one hydrochloride | HCID 25210510 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Naphthalen-2-ylmethyl 3-fluoro-4-oxopiperidine-1-carboxylate | HCID 66782177 | 60% |
Reaction Steps
To a suspension of 3-fluoropiperidin-4-one hydrochloride (35.66 g, 232.2 mmol) in THF (800 mL) at 0° C. was added a solution of NaHCO3 (46.81 g, 557.3 mmol) in water (800 mL). After most of the bubbling had subsided the ensuing solution was treated with a solution of naphthalen-2-ylmethyl carbonochloridate (56.36 g, 255.4 mmol) in THF (300 mL) dropwise, over 30 minutes. The mixture was allowed to warm to ambient temperature over 16 hours with vigorous stirring. The mixture was diluted with water and extracted with EtOAc. The combined organic phases were washed with brine, then dried over Na2SO4, filtered arid concentrated. The residue was triturated with methanol and the resulting solid was filtered and dried in vacuo to afford 41.8 g (60%) of desired product as a cream-colored powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138181B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-1194c27dd7d74a8aa378bb923577d634 |
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| Source note | uspto-grants-2012_03 |
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