HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(Phenylsulfamoyl)phenyl 4-(2-bromoethyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-hydroxy-N-phenylbenzenesulfonamide | HCID 9921239 | — |
| Reactant | 4-(2-Bromoethyl)benzoyl chloride | HCID 14092098 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Phenylsulfamoyl)phenyl 4-(2-bromoethyl)benzoate | HCID 20441809 | 86.2% |
Reaction Steps
To a mixture of 24.93 g (0.10 mol) of N-phenyl-4-hydroxybenzenesulfonamide, 10.12 g (0.10 mol) of triethylamine and 150 ml of methylene chloride was added, dropwise, a solution of 24.75 g (0.10 mol) of 4-(2-bromoethyl)benzoyl chloride in 150 ml of methylene chloride over a period of 12 minutes. The reaction mixture was stirred at room temperature for 3 hours, after which 500 ml of methylene chloride were added. The solution was washed once with 2% HCl and twice with water, dried over magnesium sulfate and concentrated to a white solid. Recrystallization from ethanol gave 39.7 g (86.1% of theory) of 4-(N-phenylsulfamoyl)phenyl 4-(2-bromoethyl)benzoate, mp=156°-7° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420630 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-f8f68397a7be45b4996ada6d610e9266 |
| Source note | uspto-grants-1983_12 |