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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053388Generated: October 31, 2026

Ammonium Chloride → (+/-)-3-(3-Aminophenyl)-5-(2,6-dichlorophenyl)-2-isoxazoline

https://huagongshe.com/reaction/2053388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(+/-)-5-(2,6-Dichlorophenyl)-3-(3-nitrophenyl)-2-isoxazolineHCID 69221841—
CatalystIronHCID 23925—
SolventWater ethanolHCID 19096565—
Product(+/-)-3-(3-Aminophenyl)-5-(2,6-dichlorophenyl)-2-isoxazolineHCID 69222917—

Reaction Conditions

Temperature80 °C

Reaction Steps

Iron powder (99 mg, 1.78 mmol) was added into a suspension of (±)-5-(2,6-dichlorophenyl)-3-(3-nitrophenyl)-2-isoxazoline (100 mg, 0.297 mmol) in ethanol/water (2/1) under nitrogen. The mixture was stirred for 10 min, followed by the addition of ammonium chloride (32 mg, 0.594 mmol). The reaction was stirred for 20 min at room temperature, followed by heating at 80° C. for 1.5 h. The reaction mixture was cooled to room temperature and filtered through a plug of Celite. The filtrate was concentrated. The residue was dissolved in ethyl acetate and washed with aqueous sodium bicarbonate solution. The ethyl acetate layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by column chromatography on silica gel, eluting with 8:2 hexanes-ethyl acetate to provide the title compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326790B2
Source datasetuspto-grants-2008_02
ORD IDord-6456801a2c2d40c28209e30cae4de906
Source noteuspto-grants-2008_02