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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063960Generated: November 1, 2026

Hydrochloric Acid → 2-[(Methylsulfonyl)methyl]piperidine

https://huagongshe.com/reaction/1063960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 14958256HCID 14958256—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
Product2-[(Methylsulfonyl)methyl]piperidineHCID 2227521390.2%

Reaction Steps

2-(Methylsulfonylmethyl)pyridine (4.40 g, 0.0257 moles) and PtO2 (0.50 g) were suspended in ethanol (80 mL) with 1N HCl (15 mL). The mixture was hydrogenated at 50 psi for 18 hours. The catalyst was filtered and the solvent removed. The residue was dissolved in CH2Cl2 and washed with sat. Na2CO3. The aqueous layer was extracted with CH2Cl2 (3×25 mL). The organic layers were combined and dried over Na2SO4 and evaporated to give a yellow oil (4.11 g, 90%) which solidified on standing. Further purification was unnecessary. LCMS (178, M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967196B1
Source datasetuspto-grants-2005_11
ORD IDord-13eb0f30e9ec42dd90368c66d1a9a5ac
Source noteuspto-grants-2005_11