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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181060Generated: November 1, 2026

Hydroxy azide → tert-butyl N-hydroxycarbamate

https://huagongshe.com/reaction/2181060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxy azideHCID 18670949—
ReactantTert-butyldicarbonateHCID 22064466—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Producttert-butyl N-hydroxycarbamateHCID 9753439.2%

Reaction Steps

A solution of 15a (9.85 g, 69.8 mmol) and t-butyldicarbonate (18.3 g, 83.8 mmol) in 50 mL of MeOH was placed in a Parr bottle with 20% Pd(OH)2 (2.0 g) and hydrogenated under 50 psi of H2 overnight. The reaction mixture was filtered through a sintered glass funnel and concentrated on a rotary evaporator. The residue was triturated with ether and the solid was collected and dried to give 3.64 g (24% yield) of Boc-amino alcohol 15b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890915B2
Source datasetuspto-grants-2005_05
ORD IDord-d1ffc1979063447796ecd1b9b595fed9
Source noteuspto-grants-2005_05