HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Hydrochloric Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl 2-(chlorosulfonyl)-6-fluorobenzoate | HCID 14257491 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | 4-Fluoro-2,3-dihydro-1lambda6,2-benzothiazole-1,1,3-trione | HCID 14257492 | — |
Reaction Steps
At 20° to 28° C. and while stirring, 42.5 g of ammonia was gassed into a mixture of 252.6 g (1 mol) of methyl 2-chlorosulfonyl-6-fluorobenzoate in 700 ml of anhydrous tetrahydrofuran. After the mixture had been stirred for an hour at 25° C., the precipitate was filtered off, dissolved in water, and extracted once with ethyl acetate. Acidification of the aqueous phase with concentrated hydrochloric acid gave 4% of theory of 4-fluoro-1,2-benzisothiazol-3-one-1,1-dioxide of m.p. 210° to 212° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05100459 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-16c167fb9268437b80a37b278d774aa7 |
| Source note | uspto-grants-1992_03 |