HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Potassium Fluoride → P-[Tetrahydropyran-2-yloxy]phenylacetylene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Edukt | Silane, trimethyl[[4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]ethynyl]- | HCID 10540306 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | P-[Tetrahydropyran-2-yloxy]phenylacetylene | HCID 11310191 | — |
Reaktionsschritte
KF (9.3 g, 160 mmol) was added to a stirred solution of 2 (22.6 g, 80 mmol) in MeOH (150 ml). The reaction mixture was stirred at room temperature for about 4 hours. After the reaction finshed (GC shows no starting material remaining), the solvent was removed under reduced pressure on a rotary evaporator. The residue was purified by column chromatography on silica gel (petroleum ether-ethyl acetate=9:1) to give a pale yellow crystals of 3. Yield 15.7 g(97%); mp 65° C., δH(CDCl3; 300 MHz): 7.42(d, J=8.7, 2H, Ar—H), 7.00(d, J=8.7, 2H, Ar—H), 5.43(t, J=3.2, 1H, OCHO), 3.87(m, 1H, THP, 3.60(m, 1H, THP), 2.99(s, 1H, C═C—H), 1.96˜1.56(m, 6H, THP).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06599945B2 |
| Quelldatensatz | uspto-grants-2003_07 |
| ORD ID | ord-bb1b2d5080344d65950a48c5889fad1f |
| Quellennotiz | uspto-grants-2003_07 |