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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,4-Dichlorophenoxy)Acetic AcidHCID 1486—
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantEthyl 3-(3-amino-4-methoxyphenyl)-2-isopropoxypropanoateHCID 22494286—
SolventTetrahydrofuranHCID 8028—
Product3-{3-[2-(2,4-Dichlorophenoxy)acetylamino]-4-methoxyphenyl}-2-isopropoxypropanoic acidHCID 577195238.2%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544835B2
Source datasetuspto-grants-2009_06
ORD IDord-732e35fd889f415092ab96ba38c09a7f
Source noteuspto-grants-2009_06