HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrobenzene → 1-n-Octylsulfonylamino-8-(1'-ethylhexanoylamino)anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | 4-Chlorooctan-3-one | HCID 12642228 | — |
| Reactant | 1-(n-Octylsulfonylamino)-8-aminoanthraquinone | HCID 19818006 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-n-Octylsulfonylamino-8-(1'-ethylhexanoylamino)anthraquinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05034547 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-8197cbd2d89e4ecabeead3476c579b88 |
| Source note | uspto-grants-1991_07 |