HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,3-Difluoro-6-nitro-(2-p-toluenesulfonyloxypropyl)oxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,3-Difluoro-6-nitro-[(2-hydroxypropyl)oxy]benzene | HCID 14697186 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2,3-Difluoro-6-nitro-(2-p-toluenesulfonyloxypropyl)oxybenzene | HCID 14697194 | 87.2% |
Reaction Steps
To a solution of 4.5 g of the compound obtained in Example 5 in 8.6 ml of pyridine was added 4.36 g of p-toluenesulfonyl chloride and the mixture was stirred under cooling with ice for 4 hours, and then at room temperature for 4 hours. To the mixture were added ethyl acetate and 1 N hydrochloric acid. The mixture was shaken, and the organic layer was separated. The organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified through silica gel column chromatography to yield 6.52 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05136059 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-c9befeeaef754feabada5e183d0022f7 |
| Source note | uspto-grants-1992_08 |