HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichlobenil → HCID 21100330, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichlobenil | HCID 3031 | — |
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | HCID 178476573 | HCID 178476573 | — |
| Product | HCID 21100330 | HCID 21100330 | — |
Reaction Steps
2,6-Dichlorobenzonitrile and 4-nitrophenyl methyl ketone can be reacted with phenyliodine (III) diacetate and trifluoromethylsulfonic acid by the method of R. S. Varma, et al, J. Heterocyclic Chem., 1998, 35(6), 1533-1534 to give 2-(2,6-dichlorophenyl)-5-(4-nitrophenyl)-1,3-oxazole. The nitrophenyl group can be reduced to the corresponding aniline with tin (II) dichloride or iron powder and ammonium chloride. Reaction of this aniline with 2,2-dichloroacetyl chloride and triethylamine can then give 2,2-dichloro-N-[4-[2-(2,6-dichlorophenyl)-5-(1,3-oxazolyl)]phenyl]acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326790B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-ec63b91ae52146d7a05400cdc52ac664 |
| Source note | uspto-grants-2008_02 |