HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269768Generated: October 30, 2026
Acetic Acid → 3-(2-Amino-4,5-dimethoxyphenyl)-2-methyl-2-propenoic acid ethyl ester
https://huagongshe.com/reaction/2269768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-(4,5-Dimethoxy-2-nitrophenyl)-2-methyl-2-propenoic acid ethyl ester | HCID 70216965 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(2-Amino-4,5-dimethoxyphenyl)-2-methyl-2-propenoic acid ethyl ester | HCID 70213112 | 78% |
Reaction Steps
Into 250 ml of glacial acetic acid, 19.0 g of 3-(4,5-dimethoxy-2-nitrophenyl)-2-methyl-2-propenoic acid ethyl ester were dissolved; and, with 15.0 g of iron powder and 20 ml of ion-exchanged water being added thereto, the mixture was refluxed under heating for 40 minutes. The resulting reaction liquid was filtered out, the filtrate was concentrated under a reduced pressure, and thus obtained residue was dissolved in ethyl acetate. The resulting product was successively washed with water, a 5% aqueous sodium hydrogencarbon ate solution, and a saturated aqueous sodium chloride solution; and then was left on sodium sulfate anhydride for one night so as to be dried. Ethyl acetate was evaporated under a reduced pressure from this solution, and the resulting crude product was recrystallized from hexane/ethanol, whereby 12.5 g of the aimed product were obtained (yield: 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329546B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-4c889f57288741eb805a246cf407934c |
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| Source note | uspto-grants-2001_12 |
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