HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → (e)-1-Fluoro-4-tosyloxy-2-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | (e)-1,4-Ditosyloxy-2-butene | HCID 18320921 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (e)-1-Fluoro-4-tosyloxy-2-butene | HCID 18320920 | 38.4% |
Reaction Steps
To a solution of (E)-1,4-ditosyloxy-2-butene (256 mg, 0.64 mmol) in 10 mL of THF was added Bu4NF (0.7 mL, 1M in THF, 0.7 mmol). The mixture was heated to reflux for 30 min. Evaporation and purification of the residue by flash column chromatography with hexane:ether/2:1 afforded the product as a colorless oil (60 mg, 38%). 1 H NMR (CDCl3, 300 MHz) δ 7.80 (d, J=8.4 Hz, 2H), 7.36 (d, J=8.4 Hz, 2H), 5.99-5.75 (m, 2H, 4.84 (ddd, JFCH=46.5 Hz, J=4.8, 1.2 Hz, 2H), 4.59-4.56 (m, 2H), 2.46 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06344179B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-800ec848f55848a9a97516fa3e9a58dd |
| Source note | uspto-grants-2002_02 |