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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746424Generated: October 25, 2026

Hydrochloric Acid → 4-Cyclopentyloxy-3-hydroxybenzaldehyde

https://huagongshe.com/reaction/746424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromocyclopentaneHCID 8728—
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Cyclopentyloxy-3-hydroxybenzaldehydeHCID 1672614967%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 3,4-dihydroxybenzaldehyde (5.0 gm, 0.0362 mol), anhydrous potassium carbonate (6.0 gm, 0.0434 mol) and cyclopentyl bromide (6.5 gm, 0.0434 mol) in dry DMF (50 ml) was heated and stirred at 80° C. for 24 hrs. Reaction mixture was then cooled and diluted with water (500 ml), acidified with 1N HCl and extracted with ethyl acetate (3×100 ml). The ethyl acetate extract was washed 5% sodium bicarbonate and brine and dried over anhydrous sodium sulfate. The dried extract on concentration afforded a residue which was purified by silica gel chromatography using 10% ethyl acetate in petroleum ether as the eluent to provide 5.0 gm of the title product as white solid. mp: 87-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393846B2
Source datasetuspto-grants-2008_07
ORD IDord-4371ba8580f9421dab962a92d0bbb1e4
Source noteuspto-grants-2008_07