HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethyl-1H-imidazole-1-sulfonamide → HCID 23510467, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethyl-1H-imidazole-1-sulfonamide | HCID 395751 | — |
| Reactant | 4-(2-Methylphenyl)benzaldehyde | HCID 1393607 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23510467 | HCID 23510467 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A suspension of N,N-dimethyl-1H-imidazole-1-sulfonamide (2.02 g) in THF (50 mL) was cooled to −78° C., and thereto was added dropwise n-BuLi (4.77 mL, 2.66 M hexane solution), and the mixture was stirred for 30 minutes. To the mixture was added p-tolyl benzaldehyde (2.08 g), and the mixture was warmed to room temperature over a period of 1 hour, and then stirred for 16 hours. The mixture was extracted with aqueous hydrochloric acid solution, washed with Et2O, and basified with an aqueous NaOH solution. This solution was extracted with Et2O, and the organic layer was dried and filtered. The solvent was evaporated under reduced pressure to give 2-[hydroxy(4-methylphenyl)methyl]-N,N-dimethyl-1H-imidazole-1-sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06759429B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-8f0cad57b2bc4efd9f8c372b40be3cff |
| Source note | uspto-grants-2004_07 |