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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494957Generated: October 30, 2026

Allyl bromide → 7-Allyloxy-5-hydroxy-2,2-dimethyl-4-oxochromane

https://huagongshe.com/reaction/494957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant5,7-Dihydroxy-2,2-dimethylchroman-4-oneHCID 821362—
SolventAcetoneHCID 180—
Product7-Allyloxy-5-hydroxy-2,2-dimethyl-4-oxochromaneHCID 5768283386.5%

Reaction Steps

2.81 g of 5,7-dihydroxy-2,2-dimethyl-4-oxochromane was dissolved in 60 ml of acetone. Thereafter, 2.05 g of potassium carbonate and 1.80 g of allyl bromide were added to the reaction solution, and the obtained mixture was then stirred at room temperature for 24 hours. Thereafter, 0.20 g of potassium carbonate and 0.18 g of allyl bromide were further added to the reaction solution, and the obtained mixture was then stirred at room temperature for 10 hours. Thereafter, 0.20 g of potassium carbonate and 0.18 g of allyl bromide were further added to the reaction solution, and the obtained mixture was then stirred at room temperature for 14 hours. Thereafter, 0.20 g of potassium carbonate and 0.18 g of allyl bromide were further added to the reaction solution, and the obtained mixture was then stirred at room temperature for 7 hours. The reaction solution was concentrated under a reduced pressure, and the residue was diluted with ethyl acetate. The resultant product was washed with water and a saturated sodium chloride aqueous solution. The organic layer was dried over magnesium sulfate and then concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), so as to obtain 2.90 g of the subject compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538123B2
Source datasetuspto-grants-2009_05
ORD IDord-c7999aea152644caa9e29bc854c35291
Source noteuspto-grants-2009_05