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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215670Generated: October 29, 2026

Iodine → 2-[4-(Dimethylamino)phenyl]-6-iodo-4H-1-benzopyran-4-one

https://huagongshe.com/reaction/215670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 11570311HCID 11570311—
ReactantSodium BisulfiteHCID 23665763—
SolventChloroformHCID 6212—
Product2-[4-(Dimethylamino)phenyl]-6-iodo-4H-1-benzopyran-4-oneHCID 11574659—

Reaction Steps

A chloroform solution of iodine (1 ml, 1 M) was added to a chloroform solution (5 ml) that contained compound 9 (30 mg, 0.054 mmol) at room temperature. The obtained mixture was reacted at room temperature for 30 minutes, and a saturated sodium bisulfite aqueous solution (5 ml) was then added thereto, so as to terminate the reaction. The chloroform layer was separated, and it was then dried over sodium sulfate. Thereafter, the solvent was distilled away under reduced pressure, and the residue was then subjected to silica gel column chromatography using ethyl acetate/hexane (1/9) as an elution solvent, so as to obtain a product of interest, 6-iodo-4′-dimethylaminoflavone (compound 11). Yield: 10 mg (yield constant: 47.3%) 1H NMR (300 MHz, CDCl3) δ8.54 (s, 1H), 7.92 (d, J=9.0 Hz, 1H), 7.81 (d, J=9.0 Hz, 2H), 7.29 (d, J=9.0 Hz, 1H), 6.71-6.80 (m, 3H), 3.09 (s, 6H). MS m/z 392 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08192717B2
Source datasetuspto-grants-2012_06
ORD IDord-4cc3a8d306b54112b67df2218e15704c
Source noteuspto-grants-2012_06