Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364667Generated: October 31, 2026

Allyl bromide → 1-Allyloxy-3-phenyl-7-nitronaphthalene

https://huagongshe.com/reaction/364667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Nitro-3-phenyl-1-naphtholHCID 121615—
SolventAcetoneHCID 180—
Product1-Allyloxy-3-phenyl-7-nitronaphthaleneHCID 20239659—

Reaction Steps

A mixture of 125 g of 3-phenyl-7-nitro-1-naphthol prepared in step (2), 65 g of anhydrous potassium carbonate, 95 g of allyl bromide and 1200 ml of acetone was refluxed for 4 hours with good stirring. After cooling, the mineral salts were removed by filtration and the residual organic solution was evaporated to dryness under reduced pressure. The crystals thus formed were washed with petroleum ether, filtered and dried at 80° C. under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04605697
Source datasetuspto-grants-1986_08
ORD IDord-3bd0a752f94a4d40a8fc8ab1fb0d33ad
Source noteuspto-grants-1986_08