HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-Nitro-N-(acetyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Benzenesulfonamide, 3-nitro- | HCID 67138 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Nitro-N-(acetyl)benzenesulfonamide | HCID 18957800 | — |
Reaction Steps
A solution of 3-nitrobenzenesulfonamide (615 mg) in 10 ml of dry tetrahydrofuran was cooled to 0° C. and mixed with 0.34 ml of acetic anhydride and 166 mg of 4-N,N-dimethylaminopyridine. The reaction mixture was stirred for 30 minutes, quenched with 10% citric acid solution, and diluted with ethyl acetate. The reaction mixture was extracted with ethyl acetate. The organic extracts were washed with brine, dried, concentrated in vacuo to yield 946 mg of the title compound in pure form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05220018 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-9387e865494f4e3ba1157d89058cb0af |
| Source note | uspto-grants-1993_06 |