Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404555Generated: October 31, 2026

Ethyl Acetate → HCID 178513381, compound

https://huagongshe.com/reaction/1404555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium HydroxideHCID 14923—
ReactantChlorosuccinimideHCID 31398—
Reactant2-Bromo-4-chloro-6-fluorobenzaldehyde oximeHCID 86667257—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178513381HCID 178513381—

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of N-chlorosuccinimide (8.34 g, 62.49 mmol) in DMF (25 ml) was added slowly to a solution of 2-bromo-4-chloro-6-fluoro-benzaldehyde oxime (15 g, 59.52 mmol) in DMF (50 ml) at 50° C. After completion of the addition, the reaction mixture was allowed to stir for 30 min at 50° C. The reaction mixture was then cooled to 3-5° C. and NH4OH (4.6 ml, 119 mmol) was added dropwise. During addition the temperature was maintained between 0-10° C. and the reaction mixture was stirred for another 15 minutes at the same temperature. EtOAc and brine were then added and the mixture was agitated vigorously for 10 minutes before the phases were allowed to settle. The aqueous layer was separated and extracted two times with EtOAc. The combined organic layers were dried with Na2SO4 and evaporated to obtain the title compound as off white solid (13 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912221B2
Source datasetuspto-grants-2014_12
ORD IDord-ff3453a9e74247b591ab26b4f0a29699
Source noteuspto-grants-2014_12