HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → N-methyl-N-(4-methoxybenzyl)-4-bromophenylsulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | 4-bromo-N-methylbenzene-1-sulfonamide | HCID 101215 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-methyl-N-(4-methoxybenzyl)-4-bromophenylsulfonamide | HCID 8319395 | 97.2% |
Reaction Steps
To a solution of N-methyl-4-bromophenylsulfonamide (2.5 g, 10 mmol) in DMF (20 mL) at room temperature was added in portions NaH (264 rag, 11 mmol). The mixture was stirred for 45 minutes and then p-methoxybenzylchloride (1.49 mL, 11 mmol) was added dropwise. The mixture was stirred for 1 hour, quenched with water and the precipitate which formed was collected by filtration and dried in vacuo at 60° C. to afford 3.6 g (97%) of N-methyl-N-(4-methoxybenzyl)-4-bromophenylsulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380721 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-837ab96246e345a2924952bb4685ac7b |
| Source note | uspto-grants-1995_01 |