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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41684Generated: October 25, 2026

Iodine → 4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one

https://huagongshe.com/reaction/41684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantAmmonium cerium-nitrateHCID 57418452—
Reactant5-Methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 67283443—
SolventSodium PyrosulfiteHCID 656671—
Product4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 6856900284.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

A flask is charged with 5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (3.96 g, 22 mmol), cerium ammonium nitrate (13.3 g, 24.2 mmol) and iodine (6.73 mg, 26.5 mmol) and then purged with nitrogen. Anhydrous acetonitrile (120 ml) is added, and the reaction heated to 40° C., with stirring for 2 hours. The crude reaction mixture is poured onto a saturated aqueous solution of sodium metabisulphite (250 ml) and extracted with dichloromethane (2×250 ml). The combined organics are dried over magnesium sulphate, filtered, and the solvent is removed under reduced pressure to give 4-Iodo-5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (5.70 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530667B2
Source datasetuspto-grants-2013_09
ORD IDord-6e2393f7454c4ffd9ef3a41c6f75f0c0
Source noteuspto-grants-2013_09