HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1-Bromo-2-[bis(4-fluorophenyl)methoxy]ethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4,4'-Difluorobenzhydryl alcohol | HCID 123049 | — |
| Reactant | Ethanol, 1-bromo- | HCID 14202443 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Bromo-2-[bis(4-fluorophenyl)methoxy]ethane | HCID 10568186 | 80% |
Reaction Steps
Bis(4-fluorophenyl)methanol was refluxed in toluene with an equimolar amount of bromoethanol in presence of a catalytic amount of p-toluenesulphonic acid. The mixture was refluxed for 12 hrs. in a Dean-Stark apparatus. The solvent was evaporated and the residue was dissolved in ether, washed with water (three times) and brine (three times). The organic layer was dried with sodium sulfate, filtered, concentrated and the residue was purified by distillation to obtain in 80% yield 1-bromo-2-[bis(4-fluorophenyl)methoxy]ethane, b.p. 170° C. at 0.1 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05171752 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-efd883b4a2324b6b9afe4565efce07bf |
| Source note | uspto-grants-1992_12 |