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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848152Generated: October 29, 2026

Allyl bromide → 7-(Allyloxy)-4-methyl-2H-chromen-2-one

https://huagongshe.com/reaction/848152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant4-MethylumbelliferoneHCID 5280567—
SolventAcetoneHCID 180—
Product7-(Allyloxy)-4-methyl-2H-chromen-2-oneHCID 23895298.1%

Reaction Steps

7-Hydroxy-4-methylcoumarin (70.00 g, 0.397 mol), anhydrous K2CO3 (140 g, 1.01 mol), and allyl bromide (100 ml, 1.15 mol) were added to 2.0 L of reagent grade acetone. The milky mixture was refluxed for sixteen hours with overhead stirring, allowed to cool to room temperature, and filtered. Solids were washed once with reagent grade acetone (150 ml.), the filtrate and wash combined, and the resulting combined filtrate concentrated to dryness with a rotary evaporator to obtain 7-allyloxy-4-methylcoumarin (84.2 g, 98% yield). The crude product melted at 100.0°-101.5° C. (lit. 1 101° C.), showed only one spot in TLC, and was used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04294847
Source datasetuspto-grants-1981_10
ORD IDord-a70b5fbf8043442ba20665c18fed52ef
Source noteuspto-grants-1981_10