HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → p-Hydrazinobenzenesulphonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 4-Chlorobenzenesulfonamide | HCID 66824 | — |
| Solvent | Water | HCID 962 | — |
| Product | p-Hydrazinobenzenesulphonamide | HCID 78105 | 95% |
Reaction Steps
A stirred solution of 4-chlorobenzenesulfonamide (38.33 g, 200 mmol) and anhydrous hydrazine (31.4 mL, 1.0 mol) was heated at reflux for 30 hours. After cooling to room temperature, the mixture was poured into water (500 mL) with swirling. The resulting precipitate was collected by filtration, washed thoroughly with water several times, air-dried, and dried under vacuum to give the title compound (35.5 g, 95% yield) as a white solid. Mp 169–171° C. 1H NMR (300 MHz, THF-d8) δ 7.59 (d, J=8.8 Hz, 2H), 6.77 (d, J=8.8 Hz, 2H), 6.62 (br, 1H), 5.99 (br, 2H), 3.87 (br, 2H). Mass spectrum (API-TIS) m/z 188 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087630B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-4f84ead693da4f968cd28a52005d8455 |
| Source note | uspto-grants-2006_08 |