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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichlorobenzoic Acid | HCID 5787 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86592578 | HCID 86592578 | — |
| Reactant | HCID 178476837 | HCID 178476837 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22926951 | HCID 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
| 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-62ec0cd81aaf4428bca06cb0b3ae9cbb |
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| Source note | uspto-grants-2009_06 |
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