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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844583Generated: October 29, 2026

Imidazole → 4(S)-(3,4-dichlorophenyl)-5-(imidazol-1-yl)pent-1-ene

https://huagongshe.com/reaction/844583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant4(S)-(3,4-dichlorophenyl)-5-(methanesulphonyloxy)pent-1-eneHCID 54078752—
SolventAcetonitrileHCID 6342—
Product4(S)-(3,4-dichlorophenyl)-5-(imidazol-1-yl)pent-1-eneHCID 5440253463.7%

Reaction Steps

4(S)-(3,4-Dichlorophenyl)-5-(methanesulphonyloxy)pent-1-ene (8.25 g) (see Preparation 93) and imidazole (5.3 g) were dissolved in anhydrous acetonitrile (80 ml) and the mixture heated under reflux for 6 days. The solvent was removed under reduced pressure to give a residue which was partitioned between diethyl ether and aqueous saturated sodium hydrogen carbonate solution (pH of the aqueous phase was kept >7). The phases were separated and the aqueous phase extracted with diethyl ether. The combined organic extracts were then washed with water, dried over anhydrous sodium sulphate and the solvent removed under reduced pressure to give a residue which was chromatographed on silica gel, eluting with a solvent gradient of 98:2 changing to 95:5, by volume, dichloromethane:methanol to give 4(S)-(3,4-dichlorophenyl)-5-(imidazol-1-yl)pent-1-ene (4.78 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380396B1
Source datasetuspto-grants-2002_04
ORD IDord-c56cf992caf64982b2ad9a734939fd04
Source noteuspto-grants-2002_04