HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Fluoride → 2-Ethynyl-5-hexylthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | [(5-Hexylthiophen-2-yl)ethynyl](trimethyl)silane | HCID 68743804 | — |
| Product | 2-Ethynyl-5-hexylthiophene | HCID 23522085 | — |
Reaction Steps
According to the method of S117b, ((5-hexylthiophen-2-yl)ethynyl)trimethylsilane (1 g, 3.7 mmol) was reacted with potassium fluoride (429 mg, 7.4 mmol) to give the title compound as a yellow oil following silica gel purification (hexane) (500 mg, 70%). 1H NMR (400 MHz, CDCl3) δ 7.10 (d, 1H, J=3.6 Hz), 6.64 (d, 1H, J=3.6 Hz), 2.78 (t, 2H, J=7.2 Hz) 1.68-1.55 (m, 2H), 1.36-1.28 (m, 6H), 0.89 (t, 3H, J=6.4 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410150B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-8318a5b0362b49ee8ad66d5689a14a37 |
| Source note | uspto-grants-2013_04 |