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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2-Ethoxy-4-nitrophenyl)-1H-isoindole-1,3(2H)-dione | HCID 20231440 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Amino-2-ethoxyphenyl)-1H-isoindole-1,3(2H)-dione | HCID 20231437 | 36.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04617316 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-d687e26a7f07479ea5b0988497e7a1fe |
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| Source note | uspto-grants-1986_10 |
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