HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 2,2-Bis-(3-nitro-4-tosyloxyphenyl)hexafluoropropane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,2-Bis(3-nitro-4-hydroxyphenyl)hexafluoropropane | HCID 11133683 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Bis-(3-nitro-4-tosyloxyphenyl)hexafluoropropane | HCID 14205043 | 58.5% |
Reaction Steps
11.5 g (0.205 mol) of potassium hydroxide are added to a solution of 42.6 g (0.1 mol) of 2,2-bis-(4-hydroxy-3-nitrophenyl) -hexafluoropropane and 39.1 g (0.205 mol) of p-toluenesulfonyl chloride in 300 ml of methylene chloride. The reaction mixture is then stirred at room temperature for five hours, in the course of which it turns an orange-yellow color. After precipitated potassium chloride (16 g) has been removed, the filtrate is dried over MgSO4. Removing the solvent and recrystallizing from toluene gives 43 g of 2,2-bis-(3-nitro-4-tosyloxyphenyl)-hexafluoropropane. Yield 58%; m.p. 206-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05028728 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-8278ea6522ee41d29c1029fdc085fc27 |
| Source note | uspto-grants-1991_07 |