HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → N-{5-[2-(4-Cyanophenyl)ethoxy]-2-methylphenyl}benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Amino-5-[2-(4-cyanophenyl)ethoxy]-2-methylbenzene | HCID 22033532 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-{5-[2-(4-Cyanophenyl)ethoxy]-2-methylphenyl}benzenesulfonamide | HCID 22033468 | 100% |
Reaction Steps
Benzenesulfonyl chloride (22 μL; 0.17 mmol) was added to a cold solution (ice :water temperature) of amino-5-[2-(4-cyanophenyl)ethoxy]-2-methyl-benzene (0.041 g; 0.16 mmol; from step (ii) above) in pyridine (4 mL) The reaction flask was left overnight in a refrigerator. NaHCO3/aq (sat.) was added and the solution extracted twice with EtOAc. The combined organic phases were washed with water, HCl/aq (2M) and water. Drying (MgSO4) and evaporation of the solvent in vacuo afforded 0.062 g (100%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06221898B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-e7be5e1600be4462aba977e363e80d52 |
| Source note | uspto-grants-2001_04 |