HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-[2-Nitro-5-(phenylsulfanyl)phenyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-Nitro-5-phenylthioaniline | HCID 170737 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | N-[2-Nitro-5-(phenylsulfanyl)phenyl]acetamide | HCID 20362827 | — |
Reaction Steps
6.0 G. of 2-amino-4-phenylthio-1-nitrobenzene is dissolved in 80 ml. acetic anhydride and treated with a few drops of sulfuric acid. The mixture is left at 20°-30° C for 2 hours then a little sodium acetate added and the solvent removed under vacuum. The residue is treated with water, filtered and recrystallized from methanol yielding 2-acetamido-4-phenylthio-1-nitrobenzene. This material may also be obtained by reaction of 2-acetamido-4-chloro-1-nitrobenzene with sodium phenylmercaptide essentially as described above for the free amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04011320 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-b42b2fba97f6424580eaa02c7ef887a4 |
| Source note | uspto-grants-1977_03 |