HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → p-[(1,2-Difluorovinyl)dimethylsilyl]phenetole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | p-[(Trifluorovinyl)dimethylsilyl]phenetole | HCID 19706492 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | p-[(1,2-Difluorovinyl)dimethylsilyl]phenetole | HCID 67642293 | 96.5% |
Reaction Steps
A solution of p-[(trifluorovinyl)dimethylsilyl]phenetole (12.0 g, 0.046 mol) in tetrahydrofuran is added dropwise to a stirred mixture of lithium aluminum hydride (1.75 g, 0.046 mol) in tetrahydrofuran at -5° C. The resultant reaction mixture is stirred at room temperature for 4 hours, cooled to 0° C., treated sequentially with ethyl acetate, water and dilute hydrochloric acid, and diluted with additional ether and dilute hydrochloric acid. The organic phase is separated, washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to give the title product as a yellow liquid (10.76 g) which is identified by 1H NMR analysis as a 9:1 mixture of Z:E isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05710102 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-864c5aa6b7ea4f518009be68761dde8f |
| Source note | uspto-grants-1998_01 |