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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41683Generated: October 25, 2026

Methanol → 5-Methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one

https://huagongshe.com/reaction/41683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant10-Oxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dioneHCID 59351951—
CatalystSodium tetrachloroaurateHCID 27127—
Product5-Methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 67283443—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 10-oxa-tricyclo[5.2.1.0*2,6*]decane-3,5-dione (9.97 g, 60 mmol) in methanol (200 ml) is added sodium tetrachloroaurate (597 mg, 1.5 mmol) and the reaction mixture is heated to 60° C. for 7 hours. The reaction mixture is allowed to cool down to room temperature and left to stand overnight. The reaction mixture is concentrated under reduced pressure, dissolved in ethyl acetate (200 ml) and washed with aqueous 2N sodium carbonate (100 ml), followed by saturated brine (100 ml). The organic layer is then dried over magnesium sulphate and concentrated under reduced pressure to give 5-methoxy-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (8.62 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530667B2
Source datasetuspto-grants-2013_09
ORD IDord-0037591a615e4fe095b275a6c05ed8ab
Source noteuspto-grants-2013_09