HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2,3,6-Trifluoro-1-ethylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-[2-(p-Toluenesulfonyloxy)ethyl]-2,3,6-trifluorobenzene | HCID 15631839 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3,6-Trifluoro-1-ethylbenzene | HCID 14834676 | 116.9% |
Reaction Steps
Lithium aluminum hydride (5.6 g) is suspended in dry diethyl ether (70 ml) and thereto is added dropwise with stirring a solution of 1-[2-(p-toluenesulfonyloxy)ethyl]-2,3,6-trifluorobenzene (23.3 g) in dry diethyl ether (170 ml) at below 10° C., and the mixture is stirred at room temperature for one hour. To the reaction mixture are added water (5.6 ml), 10% aqueous sodium hydroxide (10.0 ml) and water (5.6 ml) in this order, and the mixture is stirred at room temperature for 30 minutes. The resulting white precipitates are filtered off, and the filtrate is concentrated under atmospheric pressure to give 2,3,6-trifluoro-1-ethylbenzene (13.2 g), as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855292 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-b931c0841fde4b6aa7f20d32e389d94b |
| Source note | uspto-grants-1989_08 |