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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262602Generated: October 30, 2026

Sodium Azide → HCID 178514606, compound

https://huagongshe.com/reaction/262602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantHCID 178478571HCID 178478571—
SolventDimethylformamideHCID 6228—
ProductHCID 178514606HCID 17851460657.7%

Reaction Steps

A stirred suspension of 4-(2-chloroethoxymethyl)-imidazole hydrochloride (14.7 g.) sodium azide (9.8 g.) in dry dimethylformamide (103 ml.) was maintained at 95° for 5 hours and then set aside overnight at room temperature. Following dilution with water and filtration, the filtrate, was concentrated and the residue purified by chromatography on a dry column of alumina using ethanol. The product was basified with potassium carbonate (6.5 g.) in water (3 ml.) and the anhydrous residue was extracted withh isopropyl alcohol (3 × 50 ml.). Concentration of the extracts afforded 4-(2-azidoethoxymethyl)imidazole (7.2 g.). Hydrogenation of the azido compound (7.2 g.) in isopropyl alcohol (142 ml.) over platinum oxide catalyst (3.0 g.) gave 4-(2-aminoethoxymethyl)imidazole (6.48g.). A sample of the monopicrate monohydrochloride had m.p. 139°-140° (from nitromethane). (Found: C, 35.4; H, 3.8; N, 20.5; Cl, 8.8. C12H15CIN6O8 requires: C, 35.4; H, 3.7; N, 20.7; Cl, 8.7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04154844
Source datasetuspto-grants-1979_05
ORD IDord-cec897a082224474a1e4d55e0d4fc9c3
Source noteuspto-grants-1979_05