HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(4-vinylbenzoyl)-4-methoxybenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | N-[4-(2-bromoethyl)benzoyl]-4-methoxybenzenesulfonamide | HCID 67587147 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-vinylbenzoyl)-4-methoxybenzenesulfonamide | HCID 15404407 | — |
Reaction Steps
A solution of 35.85 g (0.09 mol) of N-[4-(2-bromoethyl)benzoyl]-4-methoxybenzenesulfonamide, 27.40 g (0.18 mol) of 1,8-diazabicyclo-[5.4.0]undec-7-ene (DBU) and 375 ml of THF was stirred at room temperature for 19.5 hrs. Solid formed within 30 mins. The mixture was poured into dilute HCl giving an oily precipitate which crystallized. The solid was collected, washed with water, redissolved in methylene chloride, dried over magnesium sulfate and concentrated to an oil which crystallized. The solid was collected, recrystallized from toluene, 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-cbd759d9c45c482fbeab048a3d68cc39 |
| Source note | uspto-grants-1999_02 |