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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283652Generated: October 31, 2026

Acetone → HCID 21510503, compound

https://huagongshe.com/reaction/1283652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSalicylaldehydeHCID 6998—
ReactantPotassium HydroxideHCID 14797—
Reactantp-Chlorophenacyl bromideHCID 68303—
SolventWaterHCID 962—
ProductHCID 21510503HCID 21510503—

Reaction Steps

To a solution of 15.3 g. (0.125 mol.) of salicylaldehyde in 100 ml. of acetone was added 7.0 g. (0.125 mol.) of potassium hydroxide dissolved in a minimum amount of water. α-Bromo-p-chloroacetophenone (29.16 g., 0.125 mol.) was added dropwise with stirring and cooling (ice bath). After addition, the reaction mixture was stirred at 25° for 12 hours. The precipitate was collected by filtration, washed with water and combined with the residue remaining after concentration of the filtrate to give 2-(4'-chlorobenzoyl)-3-hydroxycoumaran which was immediately dehydrated in the presence of p-toluenesulfonic acid to yield 2-(4'-chlorobenzoyl)benzofuran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975537
Source datasetuspto-grants-1976_08
ORD IDord-0bf8ae4dc77b49cda667974a44fd62a8
Source noteuspto-grants-1976_08