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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744035Generated: October 26, 2026

Toluene → 3-Cyclohexylpropyl 3-(1H-imidazol-4-yl)propyl ether

https://huagongshe.com/reaction/744035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant15-Crown-5HCID 36336—
Reactant(3-Chloropropyl)cyclohexaneHCID 70762—
Reactantsodium 3-(1-triphenylmethyl-1H-imidazol-4-yl)propanolateHCID 23682245—
SolventDiethyl EtherHCID 3283—
Product3-Cyclohexylpropyl 3-(1H-imidazol-4-yl)propyl etherHCID 178420894—

Reaction Conditions

Temperature75 °C

Reaction Steps

5 mmol of sodium 3-[1-(triphenylmethyl)imidazol-4-yl]propoxide in 10 ml of toluene containing 0.5 mmol of 15-Crown-5 and 5 mmol of (3-chloropropyl)cyclohexane are mixed and the mixture is stirred for 24 h at 75° C. The suspension is concentrated under vacuum, the product obtained is dissolved in diethyl ether, the solution is filtered and the residue washed with petroleum ether (40°-60° C.). The filtrate obtained is concentrated and maintained for 1 h at the boiling point in a 2N aqueous/alcohol (ethanol/water) hydrochloric acid solution. The ethanol is removed under a low vacuum and the precipitate is filtered under vacuum. The solution is basified, extracted with dichloromethane and the organic phase is concentrated. The title compound obtained is recrystallized in the hydrogenmaleate form from ethanol/diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559113
Source datasetuspto-grants-1996_09
ORD IDord-00b6922018944aca9cf64b1932ec59e1
Source noteuspto-grants-1996_09