HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Ethylaniline → HCID 21193564, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Ethylaniline | HCID 11475 | — |
| Reactant | 3-(1-Tritylimidazol-4-YL) propionaldehyde | HCID 11451428 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21193564 | HCID 21193564 | — |
Reaction Steps
0.4 g (1.10 mmol) of 3-(1-triphenylmethyl-4-imidazolyl)propionaldehyde is treated with 0.13 g (1.10 mmol) of 3-ethylaniline in anhydrous toluene, and then reduced as described for Example 154 to yield 1-triphenylmethyl-4-[3-(3-ethylphenylamino)propyl]-imidazole in the form of a colourless oil. The latter is deprotected with HCl in tetrahydrofuran, and the oil obtained is converted to oxalate as described for Example 154, to yield the product, m.p. 189-191° C. after recrystallization in a mixture of 2-propanol and diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248765B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-ff2bf334d1a24008bd5507e26e508450 |
| Source note | uspto-grants-2001_06 |