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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263538Generated: November 3, 2026

HCID 19038527, compound → HCID 19038512, compound

https://huagongshe.com/reaction/263538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19038527HCID 19038527—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
ProductHCID 19038512HCID 1903851242.5%

Reaction Steps

10% Palladium carbon (0.3 g) was added to 80 ml of ethyl acetate solution containing 4.76 g of 1-benzyloxy-1-(4-nitrobenzyl)urea. The reaction mixture was stirred overnight under normal pressure in an atmosphere of hydrogen, and then insoluble materials were removed by filtration. After evaporating the solvent under a reduced pressure, the resulting residue was purified by silica gel column chromatography (eluant: chloroform:methanol=10:1) to obtain 1.82 g of 1-(4-aminobenzyl)-1-benzyloxyurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643931
Source datasetuspto-grants-1997_07
ORD IDord-74af148fb31e44d3b2b22c07ee413027
Source noteuspto-grants-1997_07