HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methoxybenzenesulfonamide → N-[4-(2-bromoethyl)benzoyl]-4-methoxybenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methoxybenzenesulfonamide | HCID 70789 | — |
| Reactant | 4-(2-Bromoethyl)benzoyl chloride | HCID 14092098 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-[4-(2-bromoethyl)benzoyl]-4-methoxybenzenesulfonamide | HCID 67587147 | — |
Reaction Steps
A mixture of 18.72 g (0.10 mol) of 4-methoxybenzenesulfonamide, 24.75 g (0.10 mol) of 4-(2-bromoethyl)benzoyl chloride and 200 ml of toluene was stirred and heated to reflux at which time solution was achieved. The solution was heated at reflux for 16.5 hrs. The vapors emitted from the condenser were acidic during reaction. After this time, the solution was cooled and concentrated to an oil. The oil was dissolved in 3:7 heptane:toluene and cooled. Solid crystallized and was collected, washed with ligroine and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05874194 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-9502383a01704f438e73efde5cc03129 |
| Source note | uspto-grants-1999_02 |