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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733931Generated: November 1, 2026

Water → HCID 15227833, compound

https://huagongshe.com/reaction/1733931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-butyl (piperidin-4-yloxy)-acetateHCID 10036224—
ReactantHCID 15227832HCID 15227832—
ReactantHCID 19439025HCID 19439025—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 15227833HCID 15227833—

Reaction Steps

A solution of 1 g of tert-butyl 1-(3-(4-benzyloxycarbonylaminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)piperidine-4-oxyacetate (obtainable from 3-(4-benzyloxycarbonylaminomethylphenyl)-5-chloromethyl-2-oxazolidinone and tert-butyl piperidine-4-oxyacetate in accordance with the method described in Example 3) in a mixture of 38 ml of methanol, 6 ml of water and 6 ml of acetic acid is hydrogenated on 0.6 g of 5% Pd-carbon at 20° and 1 bar until H2 uptake has ceased. The mixture is filtered and the filtrate is concentrated by evaporation, and tert-butyl 1-(3-(4-aminomethylphenyl)-2-oxo-5-oxazolidinylmethyl)piperidine-4-oxyacetate is obtained, m.p. 95°-96°, FAB 420.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532255
Source datasetuspto-grants-1996_07
ORD IDord-8e1628186fad40f49a7838e9efeb025e
Source noteuspto-grants-1996_07