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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70781Generated: October 30, 2026

HCID 71268626, compound → tert-Butyl 4-(hydroxymethyl)-4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/70781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71268626HCID 71268626—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Producttert-Butyl 4-(hydroxymethyl)-4-methoxypiperidine-1-carboxylateHCID 2344730278.5%

Reaction Steps

20% palladium hydroxide on carbon (270 mg) was suspended in a MeOH (81 ml) solution of tert-butyl 4-[(benzyloxy)methyl]-4-methoxypiperidine-1-carboxylate (2.7 g), and stirred under a flow of hydrogen gas at room temperature for 4 hours. After filtering using Celite, the filtrate was concentrated, and the residue was purified by silica gel column chromatography (EtOAc) to obtain tert-butyl 4-(hydroxymethyl)-4-methoxypiperidine-1-carboxylate (1.55 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822688B2
Source datasetuspto-grants-2014_09
ORD IDord-b2e7828446454020b588376257766377
Source noteuspto-grants-2014_09