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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395015Generated: October 27, 2026

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

https://huagongshe.com/reaction/1395015

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 numberUS04201723
Source datasetuspto-grants-1980_05
ORD IDord-05dd13397a1e4142b82254cead6e31e7
Source noteuspto-grants-1980_05