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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1292133Generated: October 26, 2026

Methanol → 3-Allyloxybenzamide

https://huagongshe.com/reaction/1292133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant3-HydroxybenzamideHCID 342403—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product3-AllyloxybenzamideHCID 18354613—

Reaction Steps

To 3-hydroxybenzamide (274 mg; 2.0 mM) under a nitrogen atmosphere was added potassium carbonate (276 mg; 21.0 mM). This was dissolved in acetonitrile (20 ml) containing allyl bromide (169 ul; 2.0 mM). The mixture was refluxed for 5 hours, and the reaction followed by T.L.C.: 10% MeOH: 90% CH2Cl2. The excess solvent was then removed under vacuum, the organics extracted into dichloromethane, dried, and the solvent removed, to yield a white solid. This was recrystallised from hot water to produce a white "needle" solid (63%) as the final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05756510
Source datasetuspto-grants-1998_05
ORD IDord-50a5d18d3d824a82b3f033a1dd31d1c5
Source noteuspto-grants-1998_05