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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804448Generated: October 31, 2026

N-Iodosuccinimide → Ethyl 4-iodo-5-phenylisoxazole-3-carboxylate

https://huagongshe.com/reaction/1804448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantEthyl 5-phenylisoxazole-3-carboxylateHCID 571142—
SolventTrifluoroacetic acidHCID 6422—
ProductEthyl 4-iodo-5-phenylisoxazole-3-carboxylateHCID 5853720697.9%

Reaction Steps

Large Scale: A mixture of ethyl 5-phenylisoxazole-3-carboxylate (3.05 g, 14.0 mmol) and N-iodosuccinimide (3.79 g, 16.9 mmol) in trifluoroacetic acid (78 mL) was stirred at room temperature for 3.5 h. The volatiles were removed under reduced pressure, and the residue was partitioned between ethyl acetate (150 mL) and water (150 mL). The organic layer was washed with a 1N aqueous solution of sodium hydroxide (150 mL), washed with a 3% aqueous solution of sodium bisulfite (2×150 mL), washed with brine (150 mL), and dried over anhydrous magnesium sulfate. Concentration under reduced pressure afforded ethyl 4-iodo-5-phenylisoxazole-3-carboxylate (4.69 g, 13.7 mmol, 97% yield) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354398B2
Source datasetuspto-grants-2013_01
ORD IDord-a231e88e94a845019c2b19e57e549d25
Source noteuspto-grants-2013_01