HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1-Phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-methanesulfonyloxy-4-aza-octane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1-Phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-hydroxy-4-aza-octane | HCID 13935585 | — |
| Reactant | Acetone cyclohexane | HCID 21916603 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-methanesulfonyloxy-4-aza-octane | HCID 13935586 | — |
Reaction Steps
To a solution of 1-phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-hydroxy-4-aza-octane (56.0 g, 120 mmoles) and dry pyridine (50 mL) in dry dichloromethane (400 mL), a solution of methanesulfonylchloride (14.4 g, 1.05 equivalents) in dichloromethane is added slowly at room temperature. After stirring overnight at room temperature, the mixture is washed with 1N HCl (500 mL), 10% aqueous NaHSO3 (250 mL), and water (250 mL). Drying (Na2SO4) and evaporation of the solvent yields an oil which solidifies under oil pump vacuum. Digestion with an acetone/cyclohexane mixture gives colorless crystals of 1-phthalimido-4-p-toluenesulfonyl-7,7-difluoro-8-methanesulfonyloxy-4-aza-octane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04695654 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-d85b408c09ca4301a366ccd3a89b3420 |
| Source note | uspto-grants-1987_09 |