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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471382Generated: October 30, 2026

Triethylamine → HCID 178521337, compound

https://huagongshe.com/reaction/471382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
Reactant(2,2,2-Trifluoro-ethylcarbamoyl)-methyl-ammoniumchlorideHCID 87401929—
Reactant2-Chloro-4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-benzaldehyde OximeHCID 136386268—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178521337HCID 17852133752%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of 2-Chloro-4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-benzaldehyde oxime (i.e. the product of Step 3, 250 mg) in DMF (5 mL) was added N-chloro succinimide (80 mg) and heated to 75° C. for 1 h. After cooling, the reaction mixture was poured onto ice-water and extracted with EtOAc. The combined organic layers were washed with water, dried (Na2SO4) and concentrated in vacuo to ¼ of the original volume to obtain the crude hydroxamic acid chloride. This mixture was added to a solution of (2,2,2-trifluoro-ethylcarbamoyl)-methyl-ammoniumchloride (110 mg) and triethylamine (0.29 mL, 0.21 g) in THF (10 mL) and stirred at room temperature over night. After concentration in vacuo, the mixture was purified by chromatography on silica gel to obtain the title compound (176 mg, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633134B2
Source datasetuspto-grants-2014_01
ORD IDord-04b0a542a3e8461a9e438ced67379d70
Source noteuspto-grants-2014_01