HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 3-(Acetylamino)-5-(octadecyloxy)nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Nitro-5-(octadecyloxy)benzenamine | HCID 19388917 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Acetylamino)-5-(octadecyloxy)nitrobenzene | HCID 19389024 | 84% |
Reaction Steps
To a solution d 1.4 g (3.44 mmol) of 3-nitro-5-(octadecyloxy)benzenamine and 0.75 ml (5.4 mmol) of triethylamine in 85 ml of THF stirred in an ice bath was added 0.25 ml (3.44 mmol) of acetyl chloride. The ice bath was removed after 15 minutes and the reaction mixture was stirred at room temperature for 17 hours. Triethylamine (0.3 ml) and acetyl chloride (0.15ml ) were added and stirring was continued for 5 hours. The solvent was removed at reduced pressure and the residue was crystallized from ethyl acetate-hexane to give 1.3 g (84% yield, mp 103°-107°) of 3-(acetylamino)-5-(octadecyloxy)nitrobenzene. The structure was confirmed by nmr and mass spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446189 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-2c27bcf633944561b4c0ffa182eb7724 |
| Source note | uspto-grants-1995_08 |