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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290549Generated: October 29, 2026

Acetic Acid → 2-(4-Amino-2-ethoxyphenyl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/2290549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Ethoxy-4-nitrophenyl)-1H-isoindole-1,3(2H)-dioneHCID 20231440—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product2-(4-Amino-2-ethoxyphenyl)-1H-isoindole-1,3(2H)-dioneHCID 2023143736.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

A stirred mixture of 9.2 g (0.03 mole) of 2-(2-ethoxy-4-nitrophenyl)-1H-isoindol-1,3(2H)-dione and 12.8 g (0.23 mole) of iron powder in 50 ml of water was heated at 100° C. During a two hour period 35.1 g (0.58 mole) of glacial acetic acid was added to the hot reaction mixture. After complete addition the mixture was heated at reflux for four hours. The reaction mixture was cooled then made basic by the addition of potassium carbonate. The basic mixture was extracted with 500 ml of methylene chloride. The extract was filtered, and the filtrate extracted with 300 ml of 2N hydrochloric acid. The acidic extract was made basic with cold concentrated ammonium hydroxide. The basic solution was extracted with methylene chloride. The extract was dried over anhydrous sodium sulfate, filtered, and the filtrate evaporated under the reduced pressure to produce 3.1 g of 3-ethoxy-4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)aniline as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04617316
Source datasetuspto-grants-1986_10
ORD IDord-d687e26a7f07479ea5b0988497e7a1fe
Source noteuspto-grants-1986_10