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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267231Generated: October 30, 2026

Benzyl 4-tert-butoxycarbonylmethoxy-[1,4']bipiperidinyl-1'-carboxylate → Tert-butyl([1,4']bipiperidinyl-4-yloxy)-acetate

https://huagongshe.com/reaction/2267231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-tert-butoxycarbonylmethoxy-[1,4']bipiperidinyl-1'-carboxylateHCID 66941898—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl([1,4']bipiperidinyl-4-yloxy)-acetateHCID 86261192—

Reaction Steps

A suspension of 3.08 g (7.12 mmol) benzyl 4-tert-butoxycarbonylmethoxy-[1,4′]bipiperidinyl-1′-carboxylate and 300 mg 10% Pd/C in 60 mL MeOH was hydrogenated for 2 h at 50° C. and 3447 hPa hydrogen pressure. The catalyst was removed by suction filtering and the filtrate was evaporated to dryness. The product was reacted further without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858622B2
Source datasetuspto-grants-2010_12
ORD IDord-208cc8d96b0e4dc7a8ef42807b070d86
Source noteuspto-grants-2010_12