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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809346Generated: October 27, 2026

Benzyl({1-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-4-yl}methyl)carbamate → 2H-Pyran-4-ol, 4-[[4-(aminomethyl)-1-piperidinyl]methyl]tetrahydro-

https://huagongshe.com/reaction/1809346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl({1-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-4-yl}methyl)carbamateHCID 59255048—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2H-Pyran-4-ol, 4-[[4-(aminomethyl)-1-piperidinyl]methyl]tetrahydro-HCID 5925505794%

Reaction Steps

A mixture of benzyl ({1-[(4-hydroxytetrahydro-2H-pyran-4-yl)methyl]piperidin-4-yl}methyl)carbamate as prepared in 1(1) (5.60 g, 15.5 mmol) and palladium on activated carbon (10 wt. %, 1.20 g) in methanol (250 mL) was hydrogenated at room temperature for 20 h. Then, the mixture was filtered through a pad of Celite, and the filtrate was concentrated in vacuo to give 3.30 g (94%) of the title compound as slightly yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362038B2
Source datasetuspto-grants-2013_01
ORD IDord-95be4138b2db4defbb7d504ed28b4e90
Source noteuspto-grants-2013_01