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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39332Generated: October 26, 2026

Bromocyclopentane → 4-Cyclopentyloxy-3-hydroxybenzaldehyde

https://huagongshe.com/reaction/39332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantPotassium CarbonateHCID 11430—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
Product4-Cyclopentyloxy-3-hydroxybenzaldehydeHCID 16726149—

Reaction Conditions

Temperature77.5 °C

Reaction Steps

A suspension of 3,4-dihydroxy benzaldehyde (50.0 g, 0.3623 mol), cyclopentyl bromide (135 g, 0.9058 mol) and potassium carbonate (50.0 g, 0.3623 mol) in N,N-dimethylformamide (500 mL) was stirred at about 75-80° C. for about 1.0 hr. 4×12.5 g potassium carbonate was then added after every 1.0 hr. The reaction mixture was cooled to ambient temperature and filtered to remove inorganic materials. The residue obtained after concentration of the filtrate was diluted with toluene (250 mL), and extracted with 5-10% aqueous sodium hydroxide solution (6×50 mL). The combined aqueous layer was acidified to pH about 3 to 5 by 5N aqueous hydrochloric acid solution. The solid which separated was filtered, washed with water and dried to give 4-cyclopentyloxy-3-hydroxy benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524905B2
Source datasetuspto-grants-2013_09
ORD IDord-89aa6abc2ce546009d22bfdcfac4be8d
Source noteuspto-grants-2013_09