HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985407Generated: October 29, 2026
(2,4-Dichlorophenoxy)Acetic Acid → 3-{3-[2-(2,4-Dichlorophenoxy)acetylamino]-4-methoxyphenyl}-2-isopropoxypropanoic acid
https://huagongshe.com/reaction/1985407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2,4-Dichlorophenoxy)Acetic Acid | HCID 1486 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Ethyl 3-(3-amino-4-methoxyphenyl)-2-isopropoxypropanoate | HCID 22494286 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-{3-[2-(2,4-Dichlorophenoxy)acetylamino]-4-methoxyphenyl}-2-isopropoxypropanoic acid | HCID 57719523 | 8.2% |
Reaction Steps
30 mg of Ethyl 3-(3-amino-4-methoxyphenyl)-2-isopropoxypropanoate and 20 mg of 2,4-dichlorophenoxyacetic acid were dissolved in 0.5 ml of tetrahydrofuran, and 30 mg of carbonyldiimidazole and 0.05 ml of triethylamine were added, and the mixture was stirred at 50° C. for 4 hours. The reaction mixture was then partitioned between water and ethyl acetate, and the organic layer was concentrated. The residue was dissolved in 0.6 ml of ethanol, and 0.12 ml of 5N sodium hydroxide was added, and the mixture was stirred at room temperature for 1 hour. The reaction solution was neutralized with dilute hydrochloric acid, and extracted with ethyl acetate. The organic layer was concentrated, and the residue was purified by HPLC using a reverse-phase column and a water-acetonitrile-trifluoroacetic acid elution solvent, to give 3.4 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544835B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-732e35fd889f415092ab96ba38c09a7f |
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| Source note | uspto-grants-2009_06 |
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