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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730027Generated: November 2, 2026

Imidazole → 1-[N-2-chlorophenyl-N-propyl (thiocarbamoyl)]imidazole

https://huagongshe.com/reaction/1730027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantCarbamothioic chloride, (2-chlorophenyl)propyl-HCID 21319512—
SolventTetrahydrofuranHCID 8028—
Product1-[N-2-chlorophenyl-N-propyl (thiocarbamoyl)]imidazoleHCID 54248229—

Reaction Steps

12.4 g. N-2-chlorophenyl-N-propyl(thiocarbamoyl) chloride and 6.8 g. imidazole were refluxed in 75 ml. dry tetrahydrofuran for 16 hours. A further 2 g. imidazole was then added and the heating continued for 8 hours. After separating the solid formed evaporation of the tetrahydrofuran left an oil which was dissolved in methylene chloride. The resulting organic phase was washed with water, dried with soldium sulphate and the solvent evaporated to leave an oil which crystallised on treatment with light petroleum and chilling to give the product, 1-[N-2-chlorophenyl-N-propyl (thiocarbamoyl)]imidazole, m.p. 59°-61° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03991071
Source datasetuspto-grants-1976_11
ORD IDord-78dcce6112dc4e2aaeb2b09ec17d2b79
Source noteuspto-grants-1976_11