HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-nitro-4-(N-ethyl-N-cyclohexylamino)-benzophenone → 3-amino-4-(N-ethyl-N-cyclohexylamino)-benzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-nitro-4-(N-ethyl-N-cyclohexylamino)-benzophenone | HCID 23342778 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-amino-4-(N-ethyl-N-cyclohexylamino)-benzophenone | HCID 20341208 | — |
Reaction Steps
7.1 g. of 3-nitro-4-(N-ethyl-N-cyclohexylamino)-benzophenone are dissolved in a 1:1 mixture of benzene and ethyl acetate, and 0.7 g. of palladiumized carbon are added to the mixture. The mixture is hydrogenated at room temperature and 3 atm. hydrogen pressure until the uptake of the calculated amount of hydrogen (this requires about one hour). Thereafter the catalyst is removed by filtration, and the filtrate is evaporated to dryness under reduced pressure. 6.35 g. of crude product are obtained. After recrystallization from isopropanol, 5.8 g. of pure 3-amino-4-(N-ethyl-N-cyclohexylamino)-benzophenone, melting at 106.5°-107.5° C are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989701 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-e38883a8eb6a4c1ea60532a3bc7d7dce |
| Source note | uspto-grants-1976_11 |