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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985430Generated: November 2, 2026

2,4-Dichlorobenzoic Acid → HCID 22926951, compound

https://huagongshe.com/reaction/1985430

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichlorobenzoic AcidHCID 5787—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantHCID 86592578HCID 86592578—
ReactantHCID 178476837HCID 178476837—
SolventEthyl AcetateHCID 8857—
ProductHCID 22926951HCID 22926951—

Reaction Steps

10 mg of Ethyl 3-(3-aminooxyphenyl-2-isopropoxypropionate and 7 mg of 2,4-dichlorobenzoic acid were dissolved in 0.3 ml of N,N-dimethylformamide, 0.006 ml of diethyl phosphonate cyanide and 0.05 ml of triethylamine were added, and the mixture was stirred overnight at room temperature. The reaction solution was diluted with ethyl acetate and washed with water. The organic layer was concentrated, to give ethyl 3-[3-(2,4-dichlorobenzoylaminooxy)phenyl]-2-isopropoxypropionate. This product was then dissolved in 0.4 ml of ethanol, 0.1 ml of 5N sodium hydroxide was added, and the mixture was stirred overnight at room temperature. The reaction solution was treated with 1N hydrochloric acid, extracted with ethyl acetate, and the organic layer was concentrated. The residue was purified by reverse-phase high performance liquid chromatography, to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544835B2
Source datasetuspto-grants-2009_06
ORD IDord-62ec0cd81aaf4428bca06cb0b3ae9cbb
Source noteuspto-grants-2009_06