HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Benzenesulfonamide, 2,5-dimethoxy-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 2,5-Dimethoxybenzenesulfonyl chloride | HCID 137025 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzenesulfonamide, 2,5-dimethoxy- | HCID 209044 | — |
Reaction Steps
To a stirred solution of 15.0 g (0.063 mole) of 2,5-dimethoxybenzenesulfonyl chloride in 150 mL of tetrahydrofuran was added dropwise 80 mL of ammonia (28% aqueous solution). After complete addition the mixture was allowed to stir for 1.75 hours at room temperature. Upon standing the mixture separated into two phases. The organic phase was removed from the aqueous phase and was evaporated under reduced pressure to leave a solid residue. This residue was recrystallized from hot water (125 mL) and ethanol (40 mL) to yield 13.1 g of 2,5-dimethoxyphenylsulfonamide (mp 146.5-148.5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04743291 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-9237d0d8d56e4e399868325df64a78a4 |
| Source note | uspto-grants-1988_05 |