HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Acetyl-6-chloro-3-nitrobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 2,6-Dichloro-3-nitrobenzene-1-sulfonamide | HCID 11173285 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Acetyl-6-chloro-3-nitrobenzenesulfonamide | HCID 18373445 | 79.9% |
Reaction Steps
A solution of 2,6-dichloro-3-nitrobenzenesulfonamide (2.04 g, 7.5 mmol), potassium acetate (2.21 g, 22.5 mmol) and 18-crown-6 (5.95 g, 22.5 mmol) in 50 mL of dimethyl sulfoxide was heated to 45° C., for 7 days. The mixture was acidified with 1N aq. HCl, and extracted with ethyl acetate. The organic layer was concentrated to give the crude material. Column chromatography on silica gel, eluting with ethyl acetate/hexane/acetic acid (50/49/1, v/v/v) gave the desired product (1.67 g, 76%). EI-MS (m/z) 293.1, 295.1 (M−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06500863B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-fc4e504cf23c4ab899a31e57d7238369 |
| Source note | uspto-grants-2002_12 |