HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(Acetoxymethyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 2-(Chloromethyl)benzenesulfonamide | HCID 13364627 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Acetoxymethyl)benzenesulfonamide | HCID 13097301 | — |
Reaction Steps
A mixture of 2-(chloromethyl)benzenesulfonamide (2.00 g), potassium acetate (6.0 g) and water (75 ml) was heated to reflux for 1.5 hour. The pH was adjusted to ca. 5.0 by addition of hydrochloric acid and the chilled mixture was filtered to give 1.05 of of shiny white solid, m.p. 131°-133°. 'H NMR δ(CD3)2CO 8.00-7.83 (M), 7.60-7.25 (M), 6.55 (brd s), 5.47 (s), 2.97 (brd s), 2.10 (s), consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04332611 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-439f86cf23e941daa85e51b148807256 |
| Source note | uspto-grants-1982_06 |