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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390929Generated: October 27, 2026

Ammonium Chloride → Ethyl 6-aminobenzo[d]isoxazole-3-carboxylate

https://huagongshe.com/reaction/2390929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 6-nitrobenzo[d]isoxazole-3-carboxylateHCID 66702624—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthyl 6-aminobenzo[d]isoxazole-3-carboxylateHCID 5735597849.6%

Reaction Steps

Ethyl 6-nitrobenzo[d]isoxazole-3-carboxylate (12.7 mmol), iron (53.6 mmol), and ammonium chloride (56.1 mmol) were combined and diluted with ethanol (150 mL) and water (20 mL). The resulting suspension was heated at reflux, with vigorous stirring, for 2 h. The reaction mixture was filtered through Celite, diluted with brine (200 mL), and the resulting solution was extracted with ethyl acetate (200 mL). The organic layer was washed with of brine (3×200 mL), dried (magnesium sulfate), and concentrated. The residue was purified by chromatography (20/1 petroleum ether/ethyl acetate) to provide ethyl 6-aminobenzo[d]isoxazole-3-carboxylate 49.6% yield as a orange solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273891B2
Source datasetuspto-grants-2012_09
ORD IDord-e07e620e34464f8ca485f3a72086320f
Source noteuspto-grants-2012_09