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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963243Generated: October 28, 2026

Methyl 2-(phenoxymethyl)isonicotinate → Methyl 2-(cyclohexyloxymethyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1963243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(phenoxymethyl)isonicotinateHCID 59536560—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductMethyl 2-(cyclohexyloxymethyl)piperidine-4-carboxylateHCID 5953656273.3%

Reaction Steps

Methyl 2-(phenoxymethyl)isonicotinate (2.6 g, 10.69 mmol) was dissolved in acetic acid (50 mL), then platinum(IV) oxide (0.243 g, 1.07 mmol) was added and the mixture hydrogenated in a Büchi hydrogenator at 5 bar and room temperature for 6 h. The catalyst was removed by filtration and the solvent evaporated. The residue was taken up in DCM and the organic phase was washed with satd NaHCO3. The aqueous phase was extracted with DCM and the combined organic phases were filtered through a phase separator and evaporated. Methyl 2-(cyclohexyloxymethyl)piperidine-4-carboxylate (2 g, 73%) was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-cf814eaacbf444218c2a998d618227e1
Source noteuspto-grants-2013_04