Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442508Generated: October 27, 2026

Imidazole → 2,4-Dichloro-beta-(1-imidazolyl)propiophenone

https://huagongshe.com/reaction/442508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDiethyl EtherHCID 3283—
Reactant2,4,4,6-Tetrabromocyclohexa-2,5-dienoneHCID 88433—
Reactant1-(2,4-Dichlorophenyl)prop-2-en-1-olHCID 20282616—
Reactant1-(2,4-Dichlorophenyl)prop-2-en-1-oneHCID 20282677—
Product2,4-Dichloro-beta-(1-imidazolyl)propiophenoneHCID 53694033—

Reaction Steps

7.0 g. of 2,4-dichlorophenyl vinyl ketone (prepared by Jones oxidation of 2,4-dichlorophenyl vinyl carbinol using the general method described in J. Chem. Soc. (C), 1966, p. 1972) in 350 ml. of anhydrous ether was treated with 3.5 g. of imidazole, the solution stirred overnight and then washed with water (3 × 30 ml.). The solution is dried (MgSO4) and evaporated to give 2,4-dichloro-β-(1-imidazolyl)propiophenone as an amber gum (8.65 g.). The hydrochloride salt may be precipitated from ether and recrystallized from methanol/acetone as colorless rods, m.p. 105.5°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045568
Source datasetuspto-grants-1977_08
ORD IDord-2b1a10289aac4060948347073ffdb68f
Source noteuspto-grants-1977_08