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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128003Generated: October 31, 2026

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

https://huagongshe.com/reaction/128003

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 filration 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 numberUS04258120
Source datasetuspto-grants-1981_03
ORD IDord-bec2a09f2b0e472dbe04176f4a3cf775
Source noteuspto-grants-1981_03