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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462373Generated: October 31, 2026

HCID 10461505, compound → HCID 54514397, compound

https://huagongshe.com/reaction/1462373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10461505HCID 10461505—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 54514397HCID 54514397—

Reaction Steps

A solution of 31 g of crude N-[2-(3-carbamoyl-4-hydroxyphenoxy)-ethyl]-N-[2-(3,5-dibenzyloxyphenyl)-2-hydroxy-ethyl]-benzylamine in 300 ml of methanol is hydrogenated under normal conditions over 6 g of palladium-on-charcoal catalyst (5%) until 3 mol equivalents of hydrogen have been taken up. The catalyst is filtered off, the filtrate is evaporated and the residue is dissolved in 200 ml of isopropanol. Filtering through silica gel and evaporating the filtrate yields α-[N-[2-(3-carbamoyl-4-hydroxyphenoxy)-ethyl]aminomethyl]-3,5-dihydroxy-benzyl alcohol in the form of a brownish foam. After recrystallisation from ethylacetate/methanol the compound is obtained in pure state with a melting point of 203°-205°, and contains 1/4 mol of crystal-water. The compound is characterised by the following signals in the proton nuclear magnetic resonance spectrum in hexadeuterodimethylsulfoxide as the solvent:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460580
Source datasetuspto-grants-1984_07
ORD IDord-1e849d3b9ea14ee0b59637a364f33d88
Source noteuspto-grants-1984_07