HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 15057657, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Bromo-4-fluoro-6-(trifluoromethyl)phenol | HCID 15057656 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15057657 | HCID 15057657 | — |
Reaction Steps
0.65 g (28 mmol) of sodium is dissolved in 35 ml of dry ethanol, 5.96 g (23 mmol) of 2-bromo-4-fluoro-6-(trifluoromethyl)-phenol is added and it is stirred for 20 minutes at room temperature, 7.17 g (42 mmol) of benzyl bromide is added and refluxed for 1 hour. Sodium bromide precipitates out crystalline from the solution The hot solution is filtered, the filtrate is evaporated to dryness and the residue is chromatographed on silica gel 60 with dichloromethane/hexane. 6.29 g (18 mmol) =78.3% of the theoretical yield is obtained as a predominantly crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130119 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-5a776d8a143f48ada58d09d7837f5b50 |
| Source note | uspto-grants-1992_07 |