HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Benzenesulfonamide, N-(4-nitrophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Benzenesulfonamide, N-(4-nitrophenyl)- | HCID 231837 | 99.2% |
Reaction Steps
A solution of p-nitroaniline (1 kg, 7.245 mol) in pyridine (3.6 L) was brought to 45° C. Benzenesulfonyl chloride (1.41 kg, 8 mol) was poured in over 70 minutes, while maintaining the temperature ranging from 45 to 50° C. After 1 hour at 50° C., the reaction medium was poured onto 8 kg of ice and 4.35 L of hydrochloric acid. A yellow precipitate formed and was filtered off by suction and then dissolved in 20 L of 0.5 N sodium hydroxide at 55° C. The insoluble matter was removed by filtration and the filtrate was then neutralized hydrochloric acid while still hot. A yellow precipitate formed and was filtered off by suction, reslurried in water, and then air-dried. 2 kg of product with a melting point of 137° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07347879B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-5fd1610f50784498ac1c4ad209b9d9c3 |
| Source note | uspto-grants-2008_03 |