HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)benzaldehyde → 4-Iodomethyl-5-methyl-2-(4-trifluoromethylphenyl)oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)benzaldehyde | HCID 67996 | — |
| Reactant | 2,3-Butanedione monoxime | HCID 6409633 | — |
| Reactant | 4-Iodomethyl-5-phenyl-2-p-tolyloxazole | HCID 57434504 | — |
| Product | 4-Iodomethyl-5-methyl-2-(4-trifluoromethylphenyl)oxazole | HCID 57434514 | — |
Reaction Steps
Analogously to the building block synthesis of 4-iodomethyl-5-phenyl-2-p-tolyl-oxazole, diacetylmonoxime and 4-trifluoromethylbenzaldehyde gave 4-iodomethyl-5-methyl-2-(4-trifluoromethylphenyl)oxazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335671B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-aaaecb28ef5447c7a667b1df15fc3d71 |
| Source note | uspto-grants-2008_02 |