HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 178502610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 1,3,5-Tribenzylhexahydro-1,3,5-triazine | HCID 75685 | — |
| Reactant | 2-Oxime 2,3-butanedione | HCID 6398969 | — |
| Reactant | HCID 178526278 | HCID 178526278 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 178502610 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916936B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-03f3b968665a4e2480b37a2430d3336f |
| Source note | uspto-grants-2005_07 |