HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N1-hexanoylsulfanilamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N4-Acetylsulfanilamide | HCID 8482 | — |
| Reactant | Hexanoyl chloride | HCID 67340 | — |
| Reactant | HCID 54008860 | HCID 54008860 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N1-hexanoylsulfanilamide | HCID 14338356 | — |
Reaction Steps
N1 -hexanoylsulfanilamide was prepared as follows. To a mixture of N4 -acetylsulfanilamide (55.0 g) and pyridine (54 mL) at 95° C. was added hexanoyl chloride (28.8 g) over a period of 20 min. After an additional hour the reaction mixture was cooled to room temperature and the reaction was worked up by diluting with 600 mL D.I. water and acidifying with aqueous HCl. The product of this reaction, N4 -acetyl-N1 -hexanoylsulfanilamide, was isolated by filtration and washed with D.I. water (700 mL) to afford an off-white solid. This material was carried directly to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05713988 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-4ae0af2c5247494da797655fdc01bac6 |
| Source note | uspto-grants-1998_02 |