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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754369Generated: November 3, 2026

Iodine → HCID 178432833, compound

https://huagongshe.com/reaction/1754369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantChloroformHCID 6212—
ReactantHCID 178432834HCID 178432834—
SolventAcetic AcidHCID 176—
ProductHCID 178432833HCID 178432833107.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 2-methyl-4-(trifluoromethyl)-1H-imidazole (1 g, 6.7 mmol) was added CHCl3 (4.5 mL) and AcOH (13.5 mL) followed by I2 (1.78 g, 6.99 mmol) and HIO4.2H2O (1.52 g, 6.7 mmol), and the resulting reaction mixture was stirred at 60° C. for 3 h. The reaction mixture was then poured into ice cold 10% aqueous sodium bisulphite solution (100 mL) and the aqueous layer was extracted with EtOAc (3×100 mL). The combined organic layers were washed with brine (100 mL), dried (MgSO4) and concentrated in vacuo to obtain 5-iodo-2-methyl-4-(trifluoromethyl)-1H-imidazole (1.98 g) which was used as such in next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169248B2
Source datasetuspto-grants-2015_10
ORD IDord-b79a78fc6cc248c9a7bf201f7e8a7dc8
Source noteuspto-grants-2015_10