HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminobenzophenone → (4-Benzoyl-phenyl)-(2-nitro-phenyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminobenzophenone | HCID 14346 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (4-Benzoyl-phenyl)-(2-nitro-phenyl)-amine | HCID 11347695 | — |
Reaction Steps
The product (770 mg) is obtained according to the method of stage 1 of Example 4, by using 1.5 mL of 2-fluoro-nitrobenzene and 4.2 g of 4-aminobenzophenone in the presence of 2.54 g of potassium tert-butanolate in 40 mL of DMSO.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08207373B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-7cf8a70c973d4dcf82dc4dc5f5c65bdc |
| Source note | uspto-grants-2012_06 |