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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913177Generated: November 1, 2026

Ethyl (4-{4-(ethyloxy)-1,3-dioxo-9-[(phenylmethyl)oxy]-1,3-dihydro-2H-benzo[f]isoindol-2-yl}-3-fluorophenyl)acetate → Ethyl {4-[4-(ethyloxy)-9-hydroxy-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-fluorophenyl}acetate

https://huagongshe.com/reaction/913177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (4-{4-(ethyloxy)-1,3-dioxo-9-[(phenylmethyl)oxy]-1,3-dihydro-2H-benzo[f]isoindol-2-yl}-3-fluorophenyl)acetateHCID 58012495—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl {4-[4-(ethyloxy)-9-hydroxy-1,3-dioxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-3-fluorophenyl}acetateHCID 58012505107.5%

Reaction Steps

10% Palladium on carbon (0.175 g) was suspended in ethanol (150 ml), to this was added ethyl (4-{4-(ethyloxy)-1,3-dioxo-9-[(phenylmethyl)oxy]-1,3-dihydro-2H-benzo[f]isoindol-2-yl}-3-fluorophenyl)acetate (1.75 g, 3.32 mmol). The reaction was stirred at room temperature under an atmosphere of hydrogen for 3 hours. This was filtered through a bed of celite under a blanket of argon, and washed with dichloromethane. The filtrate was evaporated to give a yellow solid (1.56 g, 3.57 mmol). LC/MS: Rt=3.50, [MH]+ 438.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026270B2
Source datasetuspto-grants-2011_09
ORD IDord-eddc7822446041f68c21dc6ac65de503
Source noteuspto-grants-2011_09