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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901733Generated: October 31, 2026

3-(4-Phenylphenoxy)-2-hydroxypropylazide → 1-Amino-3-(biphenyl-4-yloxy)propan-2-ol

https://huagongshe.com/reaction/1901733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Phenylphenoxy)-2-hydroxypropylazideHCID 21474768—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Amino-3-(biphenyl-4-yloxy)propan-2-olHCID 16642390106.9%

Reaction Steps

Hydrogen was introduced into a mixture of 2.94 g of 3-(4-phenylphenoxy)-2-hydroxypropylazide (prepared as described in Preparation 83), 0.3 g of 10% w/w palladium-on-carbon and 60 ml of ethanol for 3 hours. At the end of this time, insolubles were removed by filtration, and the filtrate was concentrated by evaporation under reduced pressure, to give 2.84 g of the title compound, melting at 137.7° to 146.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578620
Source datasetuspto-grants-1996_11
ORD IDord-858a71c8aff14678bfc57a1b9bfdc0f0
Source noteuspto-grants-1996_11