HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → Methyl 4-[[2-ethyl-4-methyl-1H-imidazol-1-yl]methyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Methyl 4-(bromomethyl)benzoate | HCID 256687 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 178437635 | HCID 178437635 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 4-[[2-ethyl-4-methyl-1H-imidazol-1-yl]methyl]benzoate | HCID 20093489 | — |
Reaction Steps
Methyl 4-[[2-ethyl-4-methyl-1H-imidazol-1-yl]methyl]benzoate compound was prepared from 2-ethyl-4-methyl-imidazole and (4-carbmethoxy) benzylbromide in an analogous fashion as described in Example 11. A solution of the above imidazole (2.17 g, 8.14 mmol), NaOAc (1.17 g), 37 % HCHO (10 mn) , and AcOH (1.2 mn) was heated under reflux for 22 hours. The solution was evaporated under vacuo, and the residue was stirred with 10 mL of 20% NaOH solution for 2 hours. It was diluted with water and the solution was extracted with CH2Cl2. The extract was washed with water, dried, and evaporated to an oil. It was chromatographed (CH2Cl2 /MeOH, 2-5%) to give 1.0 g of the desired hydroxymethyl compound as a foam. MS (CI 288 (m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389661 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-eb617010b0b044a0bf4beee044bbf93f |
| Source note | uspto-grants-1995_02 |