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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087305Generated: October 26, 2026

Nitrobenzene → 1-n-Octylsulfonylamino-8-(1'-ethylhexanoylamino)anthraquinone

https://huagongshe.com/reaction/1087305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrobenzeneHCID 7416—
Reactant4-Chlorooctan-3-oneHCID 12642228—
Reactant1-(n-Octylsulfonylamino)-8-aminoanthraquinoneHCID 19818006—
SolventMethanolHCID 887—
Product1-n-Octylsulfonylamino-8-(1'-ethylhexanoylamino)anthraquinoneHCID 131716953—

Reaction Steps

1-(n-octylsulfonylamino)-8-aminoanthraquinone (0.25g), 1-ethylhexanoyl chloride (0.5g) and nitrobenzene (5ml) were heated at reflux for 10 mins. After addition of methanol (10ml), the mixture was heated on a steam bath for a further 10 mins to destroy excess acid chloride. 0n evaporation of low-boiling material, the remaining liquid was diluted with toluene (100ml) and separated by chromatography on a silica gel column. Nitrobenzene eluted first, and the material eluted with a 50:50 mixture of toluene:ethyl acetate was collected. The solvent was evaporated and ethanol was added to the residue, which upon trituration afforded the product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034547
Source datasetuspto-grants-1991_07
ORD IDord-8197cbd2d89e4ecabeead3476c579b88
Source noteuspto-grants-1991_07