Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471384Generated: October 30, 2026

Triethylamine → 2-Chloro-4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-n-hydroxy-n'-(2,2,2-trifluoro-ethyl)-benzamidine

https://huagongshe.com/reaction/471384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
ReactantChlorosuccinimideHCID 31398—
Reactant2-Chloro-4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-benzaldehyde OximeHCID 136386268—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-n-hydroxy-n'-(2,2,2-trifluoro-ethyl)-benzamidineHCID 13589002940%

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 (81 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 the original volume to obtain the crude hydroxamic acid chloride. This mixture was added to a solution of 2,2,2-trifluoro ethylamine (57 mg) and triethylamine (0.15 mL, 0.11 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 (122 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633134B2
Source datasetuspto-grants-2014_01
ORD IDord-42b8cee9da5d4172b66a00ff47b04cc9
Source noteuspto-grants-2014_01