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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903558Generated: November 1, 2026

2-Phenylimidazole → 1-(2,6-Dichlorobenzoyl)-2-phenyl-1H-imidazole

https://huagongshe.com/reaction/1903558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylimidazoleHCID 69591—
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
SolventTetrahydrofuranHCID 8028—
Product1-(2,6-Dichlorobenzoyl)-2-phenyl-1H-imidazoleHCID 3021176—

Reaction Steps

173 g of 2-phenylimidazole are dissolved in 600 ml of tetrahydrofuran. To this solution are added dropwise at boiling temperature 129.4 g of 2,6-dichlorobenzoyl chloride, dissolved in 400 ml of tetrahydrofuran, and the mixture is refluxed for 1 hour. The phenylimidazole hydrochloride which precipitates is separated at room temperature by vacuum filtration. The solvent of the filtrate is subsequently removed in the rotary evaporator, and the residue is recrystallised from 600 ml of acetonitrile. The yield after filtration with suction, washing with acetonitrile and drying is 153 g (80.4% of theory) of the product, m.p. 116°-117° C. There are obtained by concentrating the mother liquor by evaporation a further 22.3 g (11.7% of theory) of the product, m.p. 110°-114° C. For the analysis, 3.0 g of the compound are recrystallised from 5 ml of acetonitrile, washed with acetonitrile and dried at 60° C. in vacuo; yield: 2.6 g, m.p. 117°-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436892
Source datasetuspto-grants-1984_03
ORD IDord-d27486a046ff4a49a41fe9b9cf97dec8
Source noteuspto-grants-1984_03