HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Reactant | 4-Benzyloxy-2,2-difluorobutylamine | HCID 19860694 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide | HCID 19860703 | — |
Reaction Steps
To a solution of 4-benzyloxy-2,2-difluorobutylamine (5.16 g, 20.5 mM) and triethylamine (4.4 g, 43.4 mM) in dry dichloromethane is added toluenesulfonyl chloride (4.14 g, 21.7 moles). The mixture is stirred at room temperature overnight. Additional dichloromethane is added, and the organic phase is washed with 1N HCl followed by a water wash. Drying (Na2SO4) and evaporation of the solvent yields a white solid which is dissolved in a small volume of ether. Addition of petroleum ether yields the compound, N-(4-benzyloxy-2,2-difluorobutyl)-p-toluenesulfonamide as white crystals: 7.0 g (92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04851448 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-64df84c481fa46cc918bc8e091d7c46b |
| Source note | uspto-grants-1989_07 |