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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735498Generated: October 31, 2026

Ethyl Acetate → HCID 178467550, compound

https://huagongshe.com/reaction/1735498

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 numberUS05536827
Source datasetuspto-grants-1996_07
ORD IDord-6e74a726c2ad463eaedf94d80fbf5a6f
Source noteuspto-grants-1996_07