HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-3-nitrobenzophenone → {4-[Methyl(octyl)amino]-3-nitrophenyl}(phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-3-nitrobenzophenone | HCID 41743 | — |
| Reactant | Octylmethylamine | HCID 75538 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | {4-[Methyl(octyl)amino]-3-nitrophenyl}(phenyl)methanone | HCID 23342777 | — |
Reaction Steps
A mixture of 9.25 g. of 3-nitro-4-chloro-benzophenone, 10 ml. of ethanol and 10.3 g. of N-methyl-N-octylamine is stirred at 80° to 85 °C for 30 minutes, and then the mixture is poured onto 100 ml. of ice water. The aqueous phase is extracted with 2×75 ml. of benzene. The benzene phases are combined, washed with distilled water until chloride-free, dried over anhydrous magnesium sulphate, filtered, and evaporated in vacuo. 11.57 g. of 3-nitro-4-(N-methyl-N-octylamino)-benzophenone are obtained in the form of an oily residue. On the basis of thin layer chromatographical examination, a pure, uniform product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03975390 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-f9151830feb14138aa26736c63c0ff39 |
| Source note | uspto-grants-1976_08 |