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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351065Generated: October 30, 2026

Potassium Iodide → 2-[(5-Bromopentyl)oxy]benzaldehyde

https://huagongshe.com/reaction/2351065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSalicylaldehydeHCID 6998—
Reactant1,5-DibromopentaneHCID 8100—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product2-[(5-Bromopentyl)oxy]benzaldehydeHCID 13768059—

Reaction Steps

A solution of salicylaldehyde (82 mmoles) in acetone (50 ml) was added dropwise to a refluxing solution of 1,5-dibromopentane (90.2 mmoles), potassium carbonate (90.2 mmoles) and potassium iodide (0.4 g) in acetone (200 ml). The mixture was refluxed for 18 hours, filtered and the filtrate concentrated. The residue was dissolved in ether and washed with cold 10% sodium hydroxide solution, water and brine. The organic layer was dried over magnesium sulfate and concentrated. The product was purified by flash chromatography (4% ethyl acetate/hexane) to give 2-(5-bromopentoxy)benzaldehyde. A mixture of this compound (11.1 mmoles), 4-acetyl-3-hydroxy-2-propyl phenol (11.62 mmoles) and potassium carbonate (5.55 mmoles) in acetone (30 ml) was refluxed for 5 days, stirred at room temperature for 2 days and then refluxed for 24 hours. The suspension was cooled to room temperature, filtered and the filtrate concentrated. The residue was dissolved in ethyl acetate and then washed with ice-cold 5% sodium hydroxide solution, water and brine. The dried solution was concentrated and the product flash chromatographed on silica gel and eluted with ethylacetate/hexane to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04871771
Source datasetuspto-grants-1989_10
ORD IDord-a2ad2740fd084236923c8a7145a4ab61
Source noteuspto-grants-1989_10