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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328165Generated: October 27, 2026

Allyl bromide → Ethyl 2-(3-nitro-4-allyloxyphenyl)propionate

https://huagongshe.com/reaction/328165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-(4-hydroxy-3-nitrophenyl)propanoateHCID 21444155—
SolventAcetoneHCID 180—
ProductEthyl 2-(3-nitro-4-allyloxyphenyl)propionateHCID 21444159—

Reaction Steps

A mixture of 2.39g of ethyl 2-(3-nitro-4-hydroxyphenyl)propionate, 1.45g of allylbromide and 1.65g of potassium carbonate in 20ml of acetone was refluxed for 4 hours. After cooling, the solvent was distilled under reduced pressure. The residue was dissolved in ethyl acetate and washed with water. After the solution was dried over magnesium sulfate, the solvent was distilled off. The thus obtained oily substance was purified by means of silica gel chromatography, to give the object compound in a yield of 2.51g (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016193
Source datasetuspto-grants-1977_04
ORD IDord-db37a75043164c6b8b4aa3f1463faeb9
Source noteuspto-grants-1977_04