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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81148Generated: October 30, 2026

benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate → (2R)-5-methoxy-2-methylpiperidine

https://huagongshe.com/reaction/81148

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylateHCID 86724501—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(2R)-5-methoxy-2-methylpiperidineHCID 86724502—

Reaction Steps

To benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate (345 mg, 1.31 mmol) dissolved in ethyl acetate (6.5 mL) was added palladium on carbon (139 mg, 0.13 mmol). Hydrogen gas was added via balloon, and the reaction was stirred at room temperature for 3 hours. The mixture was filtered over celite and concentrated under reduced pressure to afford (2R)-5-methoxy-2-methylpiperidine. 1H NMR (500 MHz, DMSO-d6) δ 3.33 (s, 3H), 3.23-3.13 (m, 2H), 2.66-2.59 (m, 1H), 2.03-1.97 (m, 1H), 1.47-1.40 (m, 1H), 1.39-1.28 (m, 2H), 1.08-1.04 (m, 3H), 0.91-0.79 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846657B2
Source datasetuspto-grants-2014_09
ORD IDord-da68e188e1184401a1155ec3ec4d1575
Source noteuspto-grants-2014_09