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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289027Generated: November 1, 2026

Salicylaldehyde → 2-Benzoylbenzofuran

https://huagongshe.com/reaction/1289027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
Reactant2-ChloroacetophenoneHCID 10757—
ReactantPotassium HydroxideHCID 14797—
SolventEthanolHCID 702—
Product2-BenzoylbenzofuranHCID 9580870%

Reaction Steps

24.4 g of salicylaldehyde and 300 ml of ethanol are mixed with 11.6 g of potassium hydroxide. The resulting suspension is agitated at room temperature until the potassium hydroxide is completely dissolved. Subsequently, 31 g of phenacyl chloride are added in portions to the solution, and the batch is heated under stirring in a reflux condenser for 2 hours. The crystals precipitated while cooling down to room temperature are filtered by suction, washed with water, and recrystallized from methanol. Another fraction may be obtained by evaporating the mother liquor. Yield: 70%, colourless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747508
Source datasetuspto-grants-1998_05
ORD IDord-5a78c261060a46be939ca67b6733e6c6
Source noteuspto-grants-1998_05