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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063378Generated: November 2, 2026

Tert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylate → tert-Butyl 4-(3-hydroxypropyl)tetrahydro-1(2h)-pyridinecarboxylate

https://huagongshe.com/reaction/1063378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylateHCID 69786345—
CatalystPlatinum dioxide monohydrateHCID 11139377—
SolventEthanolHCID 702—
Producttert-Butyl 4-(3-hydroxypropyl)tetrahydro-1(2h)-pyridinecarboxylateHCID 280073999.3%

Reaction Steps

1.63 g (6.83 mmol) of 4-(3-Hydroxy-prop-1-ynyl)-piperidine-1-carboxylic acid tert-butyl ester was dissolved in 50 ml of ethanol, treated with 350 mg of PtO2.H2O and hydrogenated (1 atm) for 7 h. The reaction was filtered and evaporated to give 1.65 g (99%) of 4-(3-Hydroxy-propyl)-piperidine-1-carboxylic acid tert-butyl ester, MS: 244 (MH1, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964974B2
Source datasetuspto-grants-2005_11
ORD IDord-f5ebf4c08e2443828d823c135a3afc54
Source noteuspto-grants-2005_11