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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411416Generated: November 3, 2026

Hydrochloric Acid → 1-(2,6-Difluoro-4-nitrophenyl)piperidin-4-one

https://huagongshe.com/reaction/1411416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant8-(2,6-Difluoro-4-nitrophenyl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 58031978—
SolventAcetoneHCID 180—
Product1-(2,6-Difluoro-4-nitrophenyl)piperidin-4-oneHCID 2187818381%

Reaction Conditions

Temperature50 °C

Reaction Steps

The crude 8-(2,6-difluoro-4-nitrophenyl)-1,4-dioxa-8-azaspiro[4.5]decane from the preceding procedure was dissolved in 4:1 acetone:water (100 mL). Concentrated HCl (5 mL) was added, and the resulting mixture was stirred at 50° C. for 8 hours and then cooled to room temperature. The mixture was concentrated in vacuo to approximately 20 mL, which was carefully added to concentrated aq. NaHCO3 (100 mL) and extracted with EtOAc (2×100 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated in vacuo. The crude product was triturated with Et2O and hexanes to give a bright-yellow solid that was collected and dried to provide the title compound (7.13 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921514B2
Source datasetuspto-grants-2014_12
ORD IDord-b0d6d04082fe4deea44d4d39c2cb973d
Source noteuspto-grants-2014_12