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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222432Generated: October 30, 2026

p-Aminophenylacetic acid ethyl ester → Ethyl (4-{4-(ethyloxy)-1,3-dioxo-9-[(phenylmethyl)oxy]-1,3-dihydro-2H-benzo[f]isoindol-2-yl}phenyl)acetate

https://huagongshe.com/reaction/222432

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
Reactant1-(Ethyloxy)-4-[(phenylmethyl)oxy]-2,3-naphthalenedicarboxylic acidHCID 58012480—
SolventAcetic AcidHCID 176—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl (4-{4-(ethyloxy)-1,3-dioxo-9-[(phenylmethyl)oxy]-1,3-dihydro-2H-benzo[f]isoindol-2-yl}phenyl)acetateHCID 5801761274.2%

Reaction Steps

A mixture of 1-(ethyloxy)-4-[(phenylmethyl)oxy]-2,3-naphthalenedicarboxylic acid (2.55 g, 6.97 mmol) and ethyl(4-aminophenyl)acetate (2.49 g, 13.9 mmol) were heated to 120° C. in acetic acid (20 ml) for 18 hours. The reaction mixture was diluted with brine and extracted with ethyl acetate twice. Combined organics were washed with water then dried over magnesium sulphate, the solvent evaporated to give a brown oil. This was purified by chromatography on silica gel, eluting with ethyl acetate (0-30%) in hexane to give the title compound as a peach coloured solid (2.63 g, 5.17 mmol). LC/MS: Rt=3.95, [MH]+ 510.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207213B2
Source datasetuspto-grants-2012_06
ORD IDord-b1428b02837a464a93fa45c270bb4bce
Source noteuspto-grants-2012_06