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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879030Generated: November 1, 2026

Methyl 4-[2-fluoro-3-(methylsulfonyl)-phenyl]piperidine-1-carboxylate → 4-[2-Fluoro-3-(methylsulfonyl)phenyl]piperidine

https://huagongshe.com/reaction/1879030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-[2-fluoro-3-(methylsulfonyl)-phenyl]piperidine-1-carboxylateHCID 67532655—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product4-[2-Fluoro-3-(methylsulfonyl)phenyl]piperidineHCID 5744803891%

Reaction Steps

To a solution of methyl 4-[2-fluoro-3-(methylsulfonyl)-phenyl]piperidine-1-carboxylate (0.7 g, 2.2 mmol) in ethanol (4 ml), hydrochloric acid (3 M, 10 ml) was added and the mixture was heated at reflux for 24 h. The ethanol was evaporated and the aqueous residue was basified with sodium hydroxide (5 M) and extracted with ethylacetate (3×50 ml). The combined organic phases was washed with brine (50 ml), dried (MgSO4) and evaporated to dryness to give the title compound (0.5 g, 91%). MS m/z (relative intensity, 70 eV) 257 (M+, 6), 237 (95), 208 (83), 173 (bp) 130 (69).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314126B2
Source datasetuspto-grants-2012_11
ORD IDord-0e2e4088fae84953a3fc83989aa06616
Source noteuspto-grants-2012_11