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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032466Generated: November 2, 2026

Imidazole → HCID 22165707, compound

https://huagongshe.com/reaction/1032466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium CarbonateHCID 11430—
ReactantSulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
ReactantHCID 22165695HCID 22165695—
Solventtert-ButanolHCID 6386—
ProductHCID 22165707HCID 22165707—

Reaction Steps

1-(4-trifluoromethylphenyl)-3-(1,2,4,-triazol-1-yl)propan-2-one (1.5 g), trimethylsulphoxonium iodide (1.5 g), imidazole (0.46 g), potassium carbonate (0.75 g) in tert-butyl alcohol (20 ml) was heated at φ° for 3 h. The reaction mixture was partitioned between ethyl acetate and water, and the organic layer was separated, washed with water and then brine, and dried. The dried extract was evaporated to dryness under reduced pressure, and the residue was purified by chromatography on silica, using 5% by volume methanol in chloroform as eluent. After evaporation of the solvent, the residue crystallised from a mixture of ethyl acetate and hexane to give 3-(imidazol-1-yl)1-(1,2,4-triazol-1-yl)-2(4-trifluoromethylbenzyl)-propan-2-ol, m.p. 154-155°C. (Example 30). In a similar manner there were prepared 2-(4-chlorobenzyl)-3-(imidazol-1yl)-1-(1,2,4-triazol-1-yl) propan-2-ol, m.p. 159-161° (Example 31) and 1,3-di(imidazol-1yl)-2-(4-trifluoromethylbenzyl)propan-2-ol, m.p. 177-178° (Example 32). ##STR1##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04957934
Source datasetuspto-grants-1990_09
ORD IDord-ac85b2a3559843218cc4b8e133619076
Source noteuspto-grants-1990_09