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
3.0 G. 2-amino-4-phenylthio-1-nitrobenzene (prepared according to Example XII) is dissolved in 40 ml. of acetic anhydride and two drops of sulfuric acid added. The mixture is left at room temperature for two hours then neutralized with a little sodium acetate and concentrated under vacuum. Water is added to the residue and the crude product filtered off. Recrystallization from methanol gives pure 2-acetamido-4-phenylthio-1-nitrobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04072696 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-e63217dab307430e91eec06fcc063b11 |
| Source note | uspto-grants-1978_02 |