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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387352Generated: October 30, 2026

Dimethylformamide → HCID 54037022, compound

https://huagongshe.com/reaction/1387352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
ReactantHCID 136133815HCID 136133815—
SolventDiethyl EtherHCID 3283—
ProductHCID 54037022HCID 5403702291.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

N,N-Dimethylformamide (1 ml), potassium carbonate (0.10 g, 0.74 mmol) and 5-trifluoromethyl-2-chloropyridine (0.10 g, 0.56 mmol) were added to 5-chloro-2-hydroxyphenyl 5-methyl-1,2,4-oxadiazol-3-yl ketone O-methyloxime (0.10 g, 0.37 mmol), and the mixture was stirred at 110° C. for 2 hours. After completion of the reaction, ether (100 ml) was added, and the mixture was washed with saturated brine (80 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to give 5-chloro-2-(5-trifluoromethyl-2-pyridyloxy)phenyl 5-methyl-1,2,4-oxadiazol-3-yl ketone O-methyloxime (0.14 g, 91.7%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268312B1
Source datasetuspto-grants-2001_07
ORD IDord-2c1c06f2042d41c8be4b6c7443b0723a
Source noteuspto-grants-2001_07