HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 1-(4-Chlorobutyl)-4-fluorobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 3-(4-Fluorobenzoyl)propyl chloride | HCID 19750 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 1-(4-Chlorobutyl)-4-fluorobenzene | HCID 3016889 | — |
Reaction Steps
Triethylsilane (22.5 ml; 0.141 mol) was added dropwise to a cold (~0° C.) stirring mixture of 4-chloro-4'-fluoro-butyrophenone (10 ml; 0.0613 mol) in trifluoroacetic acid (47 ml). The reaction mixture was stirred at room temperature under nitrogen for 6 hours. The reaction was quenched with brine and extracted with diethyl ether. The organic extract was dried (MgSO4) and evaporated under vacuum giving the desired compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834493 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-fd04131e36f04a06960a49b4dd1cc09f |
| Source note | uspto-grants-1998_11 |