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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260487Generated: October 30, 2026

Ethyl Acetate → HCID 178467550, compound

https://huagongshe.com/reaction/2260487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 131719227HCID 131719227—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 178467550HCID 17846755057.7%

Reaction Steps

To 4.5 mg of 6-benzyloxymethyl-1,11-dibenzyloxy-12,13-dihydro-13-(tetraacetyl-β-D-glucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione were added 1.5 ml of ethyl acetate and 9 ml of ethanol to make a solution, and the solution was subjected to hydrogenation reaction in the presence of palladium-carbon catalyst (two medical spoonsful) for 3 hours. After the reaction, the palladium-carbon was removed by filtration and washed with methanol and tetrahydrofuran. The filtrate and the washings were concentrated under reduced pressure, the residue was subjected to thin layer chromatography (Kiesel gel 60; developed with chloroform-methanol=19:1), and the desired product was scraped and extracted with methanol to give 12,13-dihydro-1,11-dihydroxy-6-hydroxymethyl-13-(tetraacetyl-β-D-glucopyranosyl)-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione (yield: 57.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478813
Source datasetuspto-grants-1995_12
ORD IDord-30a7a88210bc4a6cad5f6475447898d6
Source noteuspto-grants-1995_12