HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluidine → 4-ethoxy-N-(4-methylphenyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluidine | HCID 7813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Ethoxybenzene-1-sulfonyl chloride | HCID 3688334 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-ethoxy-N-(4-methylphenyl)benzenesulfonamide | HCID 925010 | 94% |
Reaction Steps
1-Amino-4-methylbenzene (1.821 g, 17.0 mmol) was dissolved in DCM (25 mL). N,N-Diisopropylethylamine (3.1 mL, 18.1 mmol) and 4-ethoxy-benzenesulfonyl chloride (2.50 g, 11.3 mmol) were added successively. The reaction mixture was stirred at room temperature overnight and then washed with 10% HCl (2×20 mL) and brine (1×20 mL). Organic phase was dried with sodium sulfate before filtering and removal of solvent. The desired product, e.g. 4-ethoxy-N-(4-methylphenyl)benzenesulfonamide (3.087 g, 94%), was obtained as a colorless solid, in 99.2% purity by HPLC (MaxPlot detection between 230 and 400 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312358B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-3f9de7de5b424a2083262a8f87fa9f54 |
| Source note | uspto-grants-2007_12 |