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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273913Generated: October 28, 2026

1,4-Naphthoquinone → HCID 11024734, compound

https://huagongshe.com/reaction/273913

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-NaphthoquinoneHCID 8530—
ReactantHCID 329894HCID 329894—
CatalystCuprous chlorideHCID 62652—
SolventPyridineHCID 1049—
ProductHCID 11024734HCID 1102473489.6%

Reaction Steps

0.79 g of 1,4-naphthoquinone, 1.07 g of benzyl N-butadienylcarbamate, 25 mg of copper(I) chloride and 25 ml of pyridine were stirred at 25° C. for 30 hours under a gentle stream of air and the solution was then concentrated in vacuo. The residue was taken up in chloroform, the solution was extracted with 2N hydrochloric acid and the organic phase was concentrated in vacuo. 1.60 g of 1-benzyloxycarbonylaminoanthraquinone (83% pure; 75% of theory) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387704
Source datasetuspto-grants-1995_02
ORD IDord-619a42ef13084a79878c82376376f7d1
Source noteuspto-grants-1995_02