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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627009Generated: October 31, 2026

Triethylamine → HCID 59355632, compound

https://huagongshe.com/reaction/1627009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
Reactant1,3-Dichloro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzeneHCID 23159823—
ReactantHCID 53628322HCID 53628322—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59355632HCID 5935563291.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

In dimethylformamide (40 mL), 2-ethyl-5-hydroxyiminomethylnitrobenzene (4.30 g) and N-chlorosuccinimide (2.97 g) were dissolved, and the mixture was stirred at 60° C. for 1 hour. The reaction mixture was cooled to room temperature, and thereto was added 2-(3,5-dichlorophenyl)-3,3,3-trifluoro-1-propene (3.5 g), followed by triethylamine (1.7 g), and then the mixture was stirred for 6 hours. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 5-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-ethylnitrobenzene (5.74 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785485B2
Source datasetuspto-grants-2014_07
ORD IDord-959591e2791140ecbf19607c26a0c240
Source noteuspto-grants-2014_07