HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258613Generated: October 28, 2026
3,4-Dimethoxybenzenesulfonyl chloride → HCID 178492882, compound
https://huagongshe.com/reaction/1258613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Dimethoxybenzenesulfonyl chloride | HCID 2734183 | — |
| Reactant | HCID 178509136 | HCID 178509136 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178492882 | HCID 178492882 | 50.1% |
Reaction Steps
To a solution of 5-phenyl-4H-1,2,4-triazol-3-amine (354 mg, 2 mmol) in dry pyridine (10 mL) was added 3,4-dimethoxybenzenesulfonyl chloride (529 mg, 2.23 mmol). The solution was stirred at room temperature under Argon. After 48 h, the pyridine was removed in vacuo and flashed off with toluene. The residue was partitioned between CH2Cl2 and 1M NaOH. The organic phase was washed with 1M NaOH until no turbidity was observed on rectification of a small sample. The alkaline phase was made acidic (˜pH 3) with 1M HCl and extracted with CH2Cl2. After drying over Na2SO4, the solvent was removed in vacuo to give 0.47 g crude product. The crude product was dissolved in hot HOAc (22 mL), diluted with water (9 mL) and seeded. The product was collected by filtration, washed with water, then EtOH and dried in vacuo to give 361 mg of a granular white solid, mp 245-246° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08466182B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-841623df56814f5586c02752be8f17f3 |
|---|
| Source note | uspto-grants-2013_06 |
|---|