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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842079Generated: October 30, 2026

Bromocyclopentane → 3-Cyclopentyloxy-4-methoxybenzaldehyde

https://huagongshe.com/reaction/842079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantPotassium CarbonateHCID 11430—
ReactantIsovanillinHCID 12127—
SolventDimethylformamideHCID 6228—
Product3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 273589390.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-hydroxy-4-methoxybenzaldehyde (40 g, 0.26 mol), potassium carbonate (40 g, 0.29 mol) and cyclopentyl bromide (32 ml, 0.31 mol) in dimethylformamide (0.25 l) was heated under an argon atmosphere at 100° C. After 4 hours, additional cyclopentyl bromide (8.5 ml, 0.08 mol) was added and heating was continued for 4 hours. The mixture was allowed to cool and was filtered. The filtrate was concentrated under reduced pressure and the residue was partitioned between ether and aqueous sodium bicarbonate. The organic extract was washed with aqueous sodium carbonate and was dried (potassium carbonate). The solvent was removed in-vacuo and the residue was purified by flash chromatography, eluting with 2:1 hexanes/ether to provide a pale yellow oil (52 g, 89%)[may also be distilled at ˜0.02 mm Hg].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372770B1
Source datasetuspto-grants-2002_04
ORD IDord-6f9c4a9f0a3a4bfb9a5c7505e4779307
Source noteuspto-grants-2002_04