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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77116Generated: October 29, 2026

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

https://huagongshe.com/reaction/77116

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 numberUS08835470B2
Source datasetuspto-grants-2014_09
ORD IDord-1b852534aac44d2098e808fbf8470109
Source noteuspto-grants-2014_09