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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451943Generated: November 2, 2026

Ethyl Acetate → HCID 9948882, compound

https://huagongshe.com/reaction/1451943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantHCID 19973070HCID 19973070—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 9948882HCID 994888223.4%

Reaction Steps

In 20 ml of dioxane were dissolved 300 mg of 3-(2,4-difluorophenyl)-2,2-difluoro-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)butyric acid and 110 mg of N-hydroxysuccinimide. To the resulting solution was added 200 mg of N,N'-dicyclohexylcarbodiimide. Then, the resulting mixture was subjected to reaction at 15°-25° C. for 3 hours. The reaction mixture was subjected to filtration to remove the insolubles, and 4.5 ml of a concentrated aqueous ammonia solution was added to the filtrate. The resulting mixture was subjected to reaction at 15°-25° C. for 20 hours. Then, the solvent was removed by distillation under reduced pressure. To the residue obtained were added 20 ml of ethyl acetate and 10 ml of water. The organic layer was separated, washed with a saturated aqueous sodium chloride solution, and then dried over anhydrous magnesium sulfate. Thereafter, the solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by a column chromatography (eluant: chloroform/methanol=10/1) to obtain 70 mg of 3-(2,4-difluorophenyl)-2,2-difluoro-3-hydroxy-4-(1H-1,2,4-triazol-1-yl)butanamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605921
Source datasetuspto-grants-1997_02
ORD IDord-b2af5162879b41178737a7870feb5c02
Source noteuspto-grants-1997_02