HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → HCID 13924302, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Phenylbenzene-1-sulfonamide | HCID 12371520 | — |
| Reactant | HCID 20187520 | HCID 20187520 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13924302 | HCID 13924302 | 42.9% |
Reaction Steps
2.4 g (0.01 mol ) of 3-methylphenyl 2-chloroisonicotinate, 2.3 g (0.01 mol) of 2-biphenylsulfonamide and 1.4 g (0.01 mol) of anhydrous potassium carbonate were melted under agitation at 120° to 130° C. When the generation of gaseous carbon dioxide came to an end after 30 min to 1 hr., 50 ml of water were added and, then concentrated hydrochloric acid dropwise added to acidify. The organic layer obtained by extraction with ethyl acetate was dried and then concentrated to precipitate crude crystals, which were recrystallized to 1.6 g (yield: 42.9%) of N-(2-biphenylsulfonyl)-2-chloroisonicotinamide as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04690934 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-cc57df69c42e4c2f89f56183a699e072 |
| Source note | uspto-grants-1987_09 |