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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092322Generated: November 1, 2026

1,1,1-Trifluoro-2-iodoethane → HCID 24965850, compound

https://huagongshe.com/reaction/1092322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1,1-Trifluoro-2-iodoethaneHCID 67709—
Reactant2H-Imidazol-2-oneHCID 11819039—
ReactantHCID 24964795HCID 24964795—
ProductHCID 24965850HCID 2496585014%

Reaction Steps

This material was obtained in analogy to the procedure outlined in example 23 from 4-isobutyl-1-(2-trifluoromethyl-phenyl)-1,3-dihydro-imidazol-2-one (obtained in example 18, 200 mg) by alkylation with 2,2,2-trifluoroethyl iodide (162 mg). In contrast to the other, similar reactions, alkylation occurred predominantly at C-5 instead of N-3 of the imidazolone core. Thus, this reaction yielded 4-isobutyl-5-(2,2,2-trifluoro-ethyl)-1-(2-trifluoromethyl-phenyl)-1,3-dihydro-imidazol-2-one as a light yellow solid (36 mg). MS (ESI): 367.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129423B2
Source datasetuspto-grants-2012_03
ORD IDord-c05f0ea679d449758d12f6949355b823
Source noteuspto-grants-2012_03