HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-1-butanesulfonyl-3-amino-4-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-1-butanesulfonyl-3-acetylamino-4-nitrobenzamide | HCID 18315475 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-1-butanesulfonyl-3-amino-4-nitrobenzamide | HCID 18315533 | 94.4% |
Reaction Steps
A mixture containing 6.30 g of N-1-butanesulfonyl-3-acetylamino-4-nitrobenzamide, a 10% sodium hydroxide aqueous solution, 300 ml of ethanol and 200 ml of water was stirred at room temperature for 4 hours and then at 50° C. for 3 hours. The solvent was distilled off to approximately a half volume, and the residue was adjusted to a pH of 2 with 10% hydrochloric acid. The crystals precipitated were collected, and were dried under reduced pressure to give 5.22 g of N-1-butanesulfonyl-3-amino-4-nitrobenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06352985B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-89893da8895449d29868ada3c8725e8f |
| Source note | uspto-grants-2002_03 |