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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694644Generated: November 1, 2026

Methanol → 3-Iodo-7-methoxy-4H-1-benzopyran-4-one

https://huagongshe.com/reaction/1694644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-IodosuccinimideHCID 120273—
Reactant3-(Dimethylamino)-1-(2-hydroxy-4-methoxyphenyl)prop-2-en-1-oneHCID 67278966—
SolventChloroformHCID 6212—
Product3-Iodo-7-methoxy-4H-1-benzopyran-4-oneHCID 848817—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-(dimethylamino)-1-(2-hydroxy-4-methoxyphenyl)prop-2-en-1-one (20.0 g, 90.37 mmol) in anhydrous chloroform (100 ml) at 0° C. was added N-iodosuccinimide (23.5 g, 99.22 mmol) and silica gel (40 g). The reaction mixture was stirred at 0° C. for 60 minutes, then the insoluble material filtered off. The filtrate was washed with aqueous sodium thiosulfate (0.5M, 2×50 ml), followed by brine (100 ml), then dried over sodium sulfate. The solvent was removed under reduced pressure, providing an orange solid. To this solid was added methanol (30 ml), and the mixture was sonicated, filtered, the solid washed with methanol (2×5 ml), and the solid dried under reduced pressure, to give 3-iodo-7-methoxychromen-4-one as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158810B2
Source datasetuspto-grants-2012_04
ORD IDord-3ae1e58861c744f6b2d8dfd1e5d059e9
Source noteuspto-grants-2012_04