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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448518Generated: November 1, 2026

Diphenyl Ether → 9-Methoxy-2-methyl-7h-furo[3,2-g]chromen-7-one

https://huagongshe.com/reaction/1448518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl EtherHCID 7583—
Reactant2-methyl-9-methoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-oneHCID 20380223—
CatalystPalladiumHCID 23938—
Product9-Methoxy-2-methyl-7h-furo[3,2-g]chromen-7-oneHCID 165306—

Reaction Steps

To a solution of 0.70 g. (3.02 mmoles) of 2-methyl-9-methoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one in 15 ml. of diphenyl ether was added 0.70 g. of 10% Pd/C. The mixture was heated under reflux for 6.0 hours, cooled, and filtered over Celite (washing with methanol). The methanol was removed from the filtrate by rotary evaporation, and the remaining solution of the product in diphenyl ether was diluted with 200 ml. of pet. ether. After standing overnight, the solid which separated was filtered off and washed with pet. ether to yield 9-methoxy-2-methyl-7H-furo[3,2-g][1]benzopyran-7-one. Recrystallization from ethanol afforded an analytical sample, mp 149°-150°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04180659
Source datasetuspto-grants-1979_12
ORD IDord-7cd132baa8c945c6b94a061603f711fe
Source noteuspto-grants-1979_12