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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant(Naphthalen-2-yl)methyl carbonochloridateHCID 15764399—
Reactant3-Fluoropiperidin-4-one hydrochlorideHCID 25210510—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductNaphthalen-2-ylmethyl 3-fluoro-4-oxopiperidine-1-carboxylateHCID 6678217760%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138181B2
Source datasetuspto-grants-2012_03
ORD IDord-1194c27dd7d74a8aa378bb923577d634
Source noteuspto-grants-2012_03