HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → Nitric acid--1-[3-(2,4-dichlorophenyl)-3-methyloxiran-2-yl]-1H-imidazole (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 3061545 | HCID 3061545 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Nitric acid--1-[3-(2,4-dichlorophenyl)-3-methyloxiran-2-yl]-1H-imidazole (1/1) | HCID 3061544 | — |
Reaction Steps
A mixture of tri-n-butyltin imidazole (9.28 g), 2-chloro-2-(2,4-dichlorophenyl)propionaldehyde (4.75 g) and toluene (100 ml) was heated under reflux for 5 hours. After cooling, the reaction mixture was washed with water, dried over anhydrous magnesium sulfate and evaporated to remove the solvent. The oily residue was purified by chromatography over silica gel to give 1-[1,2-epoxy-2-(2,4-dichlorophenyl)propyl]imidazole (2.35 g, yield 43.7%) as an oil. The product was dissolved in ether, and the ether solution was neutralized by adding fuming nitric acid to give crystals of 1-[1,2-epoxy-2-(2,4-dichlorophenyl)propyl]-imidazole nitrate, which were recrystallized from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04288448 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-d710e3e66a8f4335b8e325ae5143cc34 |
| Source note | uspto-grants-1981_09 |