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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506321Generated: October 30, 2026

N-Iodosuccinimide → Methyl 4-iodo-5-isobutylisoxazole-3-carboxylate

https://huagongshe.com/reaction/1506321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantMethyl 5-isobutylisoxazole-3-carboxylateHCID 3477558—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 4-iodo-5-isobutylisoxazole-3-carboxylateHCID 5837414378%

Reaction Steps

A mixture of methyl 5-isobutylisoxazole-3-carboxylate (Preparation 5A, 0.923 g, 5.04 mmol) and N-iodosuccinimide (1.247 g, 5.54 mmol) in TFA (25 mL) was stirred at room temperature overnight. The TFA was removed under reduced pressure, and the residue was diluted with dichloromethane (100 mL), washed with a saturated aqueous solution of sodium bicarbonate (2×25 mL), 2.5% aqueous solution of sodium bisulfate (25 mL), and dried over anhydrous sodium sulfate. Concentration under reduced pressure followed by purification by flash silica gel chromatography using a 5% mixture of ethyl acetate in hexane afforded methyl 4-iodo-5-isobutylisoxazole-3-carboxylate (1.21 g, 3.91 mmol, 78% yield) as a pale yellow oil. The product had an HPLC ret. time=2.40 min. (condition A); LC/MS M+1=310.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-9ba6f2216a3043f59cff1cef6078e271
Source noteuspto-grants-2015_12