HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[(Trimethylsilyl)ethynyl]-4-(trifluoromethyl)benzene → 1-Ethynyl-4-(trifluoromethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[(Trimethylsilyl)ethynyl]-4-(trifluoromethyl)benzene | HCID 4178887 | — |
| Reactant | Tetrabutylammonium Fluoride Trihydrate | HCID 11726816 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Ethynyl-4-(trifluoromethyl)benzene | HCID 4348295 | — |
Reaction Steps
This compound was prepared in a manner analogous to that of Example 1, Step C, using 19.0 grams (0.0784 mole) of 1-(4-trifluoromethylphenyl)-2-trimethylsilylethyne and 24.7 grams (0.0784 mole) of tetrabutylammonium fluoride trihydrate in 200 ml of diethyl ether. The reaction mixture was filtered through silica gel, and the silica gel was washed with diethylether. The wash and filtrate were combined and concentrated under reduced pressure yielding, 22.9 grams of ether concentrate which was predominantly 4-trifluoromethylphenylethyne.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05073564 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-5f4e144463db49f680c6d1837630187d |
| Source note | uspto-grants-1991_12 |