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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922243Generated: October 30, 2026

N-Iodosuccinimide → (4-Iodo-3-methylisoxazol-5-yl)acetic acid methyl ester

https://huagongshe.com/reaction/922243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
ReactantMethyl 2-(3-methylisoxazol-5-yl)acetateHCID 12366875—
SolventTrifluoroacetic acidHCID 6422—
Product(4-Iodo-3-methylisoxazol-5-yl)acetic acid methyl esterHCID 6668571572.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a sealed tube fitted with magnetic stirrer was charged methyl (3-methyl-1,2-oxazol-5-yl)acetate (0.9 g, 5.8 mmol) and N-iodosuccinimide (2.61 g, 11.6 mmol) in 10 mL trifluoroacetic acid. The reaction mixture was heated at 65° C. for 3 h. The RM was quenched with NaHCO3 solution (25 mL) and extracted with ethyl acetate (30 mL). The organic layer was washed with water (30 mL) and saturated brine solution (30 mL). The organic layer was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The product was obtained as brown solid (1.18 g, yield: 72.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278915B2
Source datasetuspto-grants-2016_03
ORD IDord-b802d6b9b7f54f6ba2613b59b6818ddd
Source noteuspto-grants-2016_03