HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride → HCID 59577086, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride | HCID 2776415 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59577086 | HCID 59577086 | 87% |
Reaction Steps
To a stirred solution of 4-(1,3-oxazol-5-yl)benzenesulfonyl chloride (1.00 g, 4.10 mmol) in tetrahydrofuran (15.0 mL) was added 25% ammonia water solution (5.00 mL) at room temperature. After 1 h the reaction mixture was partitioned between ethyl acetate (100.0 mL) and 1.0 N hydrochloric acid (10.0 mL) and separated. The organic layer was washed with water (2×40 mL), saturated sodium chloride (80 mL), dried (MgSO4), filtered. The filtrate was concentrated under reduced pressure to provide 4-(1,3-oxazol-5-yl)benzenesulfonamide (800 mg, 87%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586571B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-a28aad63a6414442bf5b67ddc5d3a7d7 |
| Source note | uspto-grants-2013_11 |