Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972090Generated: October 27, 2026

(3R*,4R*)-4-azido-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester → rac-tert-butyl (3R,4R)-4-amino-3-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1972090

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R*,4R*)-4-azido-3-hydroxy-piperidine-1-carboxylic acid tert-butyl esterHCID 58745530—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Productrac-tert-butyl (3R,4R)-4-amino-3-hydroxypiperidine-1-carboxylateHCID 10727458—

Reaction Steps

To a stirred solution of (±)-trans-4-azido-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (10 mmol, 2.42 g) in methanol (25 mL) was added 10% palladium on carbon (0.5 g, wet), and the resultant reaction mixture was subjected to hydrogenation using a balloon full of hydrogen for 8 h. The catalyst was filtered through a pad of celite, and the pad was with methanol (25 mL). The combined filtrate was concentrated under reduced pressure to provide (±)-trans-4-amino-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431575B2
Source datasetuspto-grants-2013_04
ORD IDord-bb5925887b554ecd9f963a8fac70750a
Source noteuspto-grants-2013_04