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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273911Generated: November 1, 2026

HCID 14614968, compound → HCID 11024734, compound

https://huagongshe.com/reaction/273911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14614968HCID 14614968—
CatalystCuprous chlorideHCID 62652—
SolventPyridineHCID 1049—
ProductHCID 11024734HCID 1102473488.2%

Reaction Steps

0.47 g of 1-benzyloxycarbonylamino-1,4,4a,9a-tetrahydroanthraquinone, 6 mg of copper(I) chloride and 10 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. 0.41 g of 1-benzyloxycarbonylaminoanthraquinone (86% pure; 76% of theory) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387704
Source datasetuspto-grants-1995_02
ORD IDord-d963fcfe3a7549d4b179f25a147e5fff
Source noteuspto-grants-1995_02