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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789487Generated: October 30, 2026

Methanol → Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1789487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylateHCID 22708806—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductEthyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylateHCID 14049029—

Reaction Steps

A mixture of 73 parts of ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate, 400 parts of methanol and 150 parts of acetic acid was hydrogenated in the Parr-apparatus with 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. To the residue was added crushed ice and the whole was alkalized with potassium hydroxide. The aqueous phase was salted out with potassium carbonate and the product was extracted with benzene. The extract was dried, filtered and evaporated, yielding 63.5 parts of ethyl 4-(aminomethyl)-4-hydroxy-1-piperidinecarboxylate; mp. ±82° C. (intermediate 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689330
Source datasetuspto-grants-1987_08
ORD IDord-446a94c66a0c4158844c2afd4599238d
Source noteuspto-grants-1987_08