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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388366Generated: October 28, 2026

Triethylamine → 1-{4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-naphthalen-1-yl}-1H-[1,2,4]triazole

https://huagongshe.com/reaction/388366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
Reactant1,3-Dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzeneHCID 23159823—
Reactant4-[1,2,4]Triazol-1-yl-naphthalene-1-carbaldehyde oximeHCID 86658156—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-{4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-naphthalen-1-yl}-1H-[1,2,4]triazoleHCID 4684239664.1%

Reaction Steps

N-chlorosuccinimid (220 mg) is added to a solution of 4-[1,2,4]triazol-1-yl-naphthalene-1-carbaldehyde oxime (390 mg) in DMF (5 ml). After 45 minutes at 40° C., the reaction is cold down to 0° C., and 1,3-dichloro-5-(1-trifluoromethyl-vinyl)-benzene (394 mg, Example 1, step A) and triethylamine (0.25 ml) are added. The reaction is then further reacted at room temperature for 3 hours. Water is added (50 ml) and the reaction mixture is extracted two times with ethyl acetate. The organic phase is extracted, with a saturated aqueous solution of NaCl, dried over Na2SO4 and concentrated in vacuo. The crude product is purified on a semi-preparative HPLC: to yield 1-{4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-naphthalen-1-yl}-1H-[1,2,4]triazole (500 mg) as beige crystals. MS (HPLC/MS): 477 (MH+). Retention time: 5.20 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377942B2
Source datasetuspto-grants-2013_02
ORD IDord-82f193da01f54203bf99b8c337c34dc2
Source noteuspto-grants-2013_02