HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 178418921, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,1-Dibromo-3,3,3-trifluoroacetone | HCID 550523 | — |
| Reactant | 2-METHYLISONICOTINALDEHYDE | HCID 2763000 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178418921 | HCID 178418921 | — |
Reaction Steps
To a solution of sodium acetate trihydrate (5.8 g.) in water (20 ml.) is added 1,1-dibromo-3,3,3-trifluoroacetone (5.9 g., 0.022 mole). The solution is heated 45 minutes at steam bath temperature and then cooled. The solution is added to a solution of 2-methylisonicotinaldehyde (2.4 g., 0.02 mole) in methanol (100 ml.) and concentrated aqueous ammonia (25 ml.). The reaction mixture is allowed to stand 4.5 hours at room temperature. The reaction mixture is concentrated under reduced pressure; an oil separates and solidifies and this is filtered (0.6 g.) after recrystallization from a mixture of water and ethanol to afford 2-methyl-4-pyridyl)-4-trifluoromethylimidazole, m.p., 195°-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125530 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-ca3e77a4d08844cd961bed2329cc7e8b |
| Source note | uspto-grants-1978_11 |