HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 42635546, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde | HCID 618233 | — |
| Reactant | HCID 694901 | HCID 694901 | — |
| Product | HCID 42635546 | HCID 42635546 | 67% |
Reaction Steps
The condensing of commercially available 1-trityl-1H-imidazole-4-carboxaldehyde (I) with phtalide to form 2-(1-trityl-1H-imidazole-4-yl)indan-1,3-dione (II) is performed under the conditions that are similar to those used for synthesis of 4-(indane-1,3-dionyl)pyridine J. Org. Chem. 1971, vol. 36, p. 1563. surprisingly, the bulky 1-trityl-1H-imidazole-4-carboxaldehyde (I) reacted as expected and produced 2-(1-trityl-1H-imidazole-4-yl)indan-1,3-dione (II) in over 67% yield. Both ethyl acetate and dioxane can be used as reaction media.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431717B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-e4fdd5e23a5b418c82829c465e7583c9 |
| Source note | uspto-grants-2013_04 |