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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584815Generated: November 2, 2026

Acetic Anhydride → HCID 178471861, compound

https://huagongshe.com/reaction/1584815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantCyclopropylamineHCID 69828—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantEthyl 4-bromo-2,5-difluoro-3-methylbenzoylacetateHCID 21220244—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 178471861HCID 178471861—

Reaction Steps

In 150 ml of methylene chloride was dissolved 30.0 g of ethyl 4-bromo-2,5-difluoro-3-methylbenzoylacetate, and 19.1 g of acetic anhydride and 22.3 g of N,N-dimethylformamide dimethyl acetal were added to the solution, after which the resulting mixture was stirred at room temperature for one hour. Thereafter, the solvent was removed by distillation under reduced pressure. The residue obtained was dissolved in 90 ml of ethanol and 5.90 g of cyclopropylamine was added thereto, after which the resulting mixture was stirred at room temperature for 30 minutes. The solvent was then removed by distillation under reduced pressure. To the residue obtained was added n-hexane and the crystals formed were collected by filtration, to obtain 35.7 g of colorless, crystalline ethyl 2-(4-bromo-2,5-difluoro-3-methylbenzoyl)-3-cyclopropylaminoacrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935952
Source datasetuspto-grants-1999_08
ORD IDord-da6ad9c6b29049c28b13c1b9c483af8a
Source noteuspto-grants-1999_08