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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357781Generated: November 2, 2026

Thionyl Chloride → 5-(azidomethyl)-1H-imidazole

https://huagongshe.com/reaction/2357781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium AzideHCID 33557—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178519868HCID 178519868—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product5-(azidomethyl)-1H-imidazoleHCID 178514575—

Reaction Steps

To a suspension of 4-hydroxymethylimidazole II-1 (1.09 g, 11.1 mmol) in CH3CN (12 mL), SOCl2 (5 mL) was added. After being stirred at room temperature for 30 min, the suspension became clear. After stirring for additional 2 h, the solution was concentrated in vacuo to give a solid, which was then dissolved in DMF (15 mL). To the solution, NaN3 (2.16 g, 33.2 mmol) was added. After the mixture was stirred at room temperature overnight, water and EtOAc were added, then 5% aq. NaHCO3 was also added. The organic layer was separated, dried over Na2SO4, concentrated in vacuo to give 4-azidomethylimidazole as a solid (0.759 g). MS 124.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763608B2
Source datasetuspto-grants-2010_07
ORD IDord-1e3f8d2ce7214f04a1dceee0be908402
Source noteuspto-grants-2010_07