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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895797Generated: October 30, 2026

Methyl iodide → HCID 178502610, compound

https://huagongshe.com/reaction/895797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,3,5-Tribenzylhexahydro-1,3,5-triazineHCID 75685—
Reactant2-Oxime 2,3-butanedioneHCID 6398969—
ReactantHCID 178526278HCID 178526278—
SolventChloroformHCID 6212—
ProductHCID 178502610HCID 178502610—

Reaction Steps

Methyl iodide (0.5 mL, 7.8 mmol) was added via syringe to a solution of imidazole-N-oxide 1 (1.0 g, 4.9 mmol) in ca. 20 mL of CHCl3 (compound 1 was prepared from 1,3,5-tribenzyl-[1,3,5]triazinane and butane-2,3-dione monooxime using the procedure of Arduengo et al. (1992), supra.) The resulting mixture was stirred at room temperature overnight. Removal of the volatiles in vacuo afforded a thick yellow oil of suitable purity in an undetermined yield. 1H-NMR (6, CDCl3): 10.32 (s, 1H, N—CH—N); 7.39 (m, 5H, C6H5); 5.56 (s, 2H, NCH2); 4.38 (s, 3H, OCH3); 2.27 (s, 3H, CH3); 2.20 (s, 3H, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916936B2
Source datasetuspto-grants-2005_07
ORD IDord-03f3b968665a4e2480b37a2430d3336f
Source noteuspto-grants-2005_07