HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 1-(Benzyloxy)-3-bromo-5-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-3,5-difluorobenzene | HCID 136313 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1-(Benzyloxy)-3-bromo-5-fluorobenzene | HCID 11254516 | 57% |
Reaction Steps
Sodium hydride (50% w/w dispersion in mineral oil, 12.4 g) was added portionwise to a mixture of benzyl alcohol (26.7 ml) and DMA (500 ml) and the mixture was stirred at ambient temperature for 1 hour. 1-Bromo-3,5-difluorobenzene (50 g) was added carefully to control the vigour of the ensuing exothermic reaction. The mixture was stirred at ambient temperature for 2 hours and the solvent was evaporated. The residue was partitioned between methylene chloride and water the organic phase was washed with water (4×50 ml), dried (MgSO4) and evaporated. The residue was purified by distillation to give 3-benzyloxy-1-bromo-5-flurobenzene (41.8 g, 57%), as a colourless liquid b.p. 124°-130 C. at 0.3 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254581 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-382211250f4a425b8df5e7128b9d6571 |
| Source note | uspto-grants-1993_10 |