HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → {2-[(Benzenesulfonyl)amino]-1,3-thiazol-4-yl}acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | ethyl {2-[(phenylsulfonyl)amino]-1,3-thiazol-4-yl}acetate | HCID 717505 | — |
| Solvent | Water | HCID 962 | — |
| Product | {2-[(Benzenesulfonyl)amino]-1,3-thiazol-4-yl}acetic acid | HCID 16394950 | 92.6% |
Reaction Steps
To an aqueous solution of potassium hydroxide (5.0 g.) in water (150 ml.) was added ethyl 2-benzenesulfonamidothiazol-4-ylacetate (9.1 g.) at 10° C. with stirring, and the mixture was stirred for 30 minutes at room temperature. The reaction mixture was adjusted to pH 4 to 4.5 with acetic anhydride, and the mixture was stirred under ice-cooling till the crystals precipitated. The crystals were collected by filtration and dried to give 2-benzenesulfonamidothiazol-4-ylacetic acid (7.7 g.), mp 94° to 96° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04254260 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-6fb2613198e844988502bf2fc789b9e0 |
| Source note | uspto-grants-1981_03 |