HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methanesulfonamide, N-(3-oxospiro(benzofuran-2(3H),1'-cyclopropan)-5-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 12925991 | HCID 12925991 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methanesulfonamide, N-(3-oxospiro(benzofuran-2(3H),1'-cyclopropan)-5-yl)- | HCID 3055476 | — |
Reaction Steps
To a solution of 5-aminospiro[benzo[b]furan-2(3H),1'-cyclopropane]-3-one (0.519 g.) in pyridine (5 ml.) was added methanesulfonyl chloride (0.28 ml.) under ice-cooling, followed by stirring. The reaction mixture was poured into cooled dilute hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried and concentrated to remove the solvent. The residue was recrystallized from ethanol. By the above procedure there was obtained 5-methylsulfonylaminospiro[benzo[b]furan-2(3H),1'-cyclopropane]-3-one as colorless needles melting at 152°-154° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284644 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-41791359b72e4a419fb5814ffd264535 |
| Source note | uspto-grants-1981_08 |