HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-(1H-imidazol-5-yl)-N-methylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 178521891 | HCID 178521891 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1H-imidazol-5-yl)-N-methylaniline | HCID 178482100 | — |
Reaction Steps
A suspension of N-[4-(imidazol-4-yl)-phenyl]-formamide (8 g) in anhydrous tetrahydrofuran (80 ml) was slowly added dropwise to a suspension of LiAlH4 (6.5 g) in anhydrous tetrahydrofuran. The reaction mixture was refluxed for 4 hours and cooled. Wet diethylether was added, and then the solution was evaporated to dryness. The residue was dissolved in water and ethylacetate. After working up the organic layer, 4.6 g of N-methyl-N-[4-(imidazol-4-yl)-phenyl]-amine, M.p. 75°-76° C., were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666932 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-6b684fa9031646028208df807f1ff6ba |
| Source note | uspto-grants-1987_05 |