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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963318Generated: October 27, 2026

Methyl 2-(3,5-difluorobenzyl)isonicotinate → Methyl 2-(3,5-difluorobenzyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1963318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(3,5-difluorobenzyl)isonicotinateHCID 66731588—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductMethyl 2-(3,5-difluorobenzyl)piperidine-4-carboxylateHCID 6673163093.3%

Reaction Steps

Methyl 2-(3,5-difluorobenzyl)isonicotinate (7.417 g, 28.18 mmol) was dissolved in acetic acid (72 mL) and platinum(IV) oxide (0.320 g, 1.41 mmol) was added. The mixture was hydrogenated in a Büchi hydrogenator at room temperature and 5 bar for 5 h. The reaction mixture was filtered through celite and the catalyst was washed with MeOH. The eluate was concentrated and DCM and 1 M K2CO3 were added. The phases were separated and the organic phase was washed with brine before it was dried and concentrated to yield methyl 2-(3,5-difluorobenzyl)piperidine-4-carboxylate (7.08 g, 93%). MS m/z 270 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-c1124d6c652f4db0ad7773f9028724bd
Source noteuspto-grants-2013_04