Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729649Generated: October 27, 2026

3-nitro-4-(N-ethyl-N-cyclohexylamino)-benzophenone → 3-amino-4-(N-ethyl-N-cyclohexylamino)-benzophenone

https://huagongshe.com/reaction/1729649

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-nitro-4-(N-ethyl-N-cyclohexylamino)-benzophenoneHCID 23342778—
ReactantHCID 178418361HCID 178418361—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product3-amino-4-(N-ethyl-N-cyclohexylamino)-benzophenoneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989701
Source datasetuspto-grants-1976_11
ORD IDord-e38883a8eb6a4c1ea60532a3bc7d7dce
Source noteuspto-grants-1976_11