HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2',4'-Dihydroxyacetophenone → 1-(2-Hydroxy-4-octyloxy-phenyl)-ethanone
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2',4'-Dihydroxyacetophenone | HCID 6990 | — |
| Edukt | 1-Bromooctane | HCID 8140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-(2-Hydroxy-4-octyloxy-phenyl)-ethanone | HCID 10468007 | — |
Reaktionsbedingungen
| Temperatur | 55 °C |
|---|
Reaktionsschritte
A slurry of 2,4-dihydroxy actophenone (3.8 g; 25 mmol) and KHCO3 (2.75 g; 27.5 mmol) in DMF (50 mL) was stirred at 50° C. for 1 hour and then added 1-bromooctane (4.75 mL; 27.5 mmol). The reaction mixture was stirred at 50-60° C. for 7 days, poured onto H2O (100 mL) and the aqueous phase extracted with diethyl ether (3×). The combined organic fractions was dried (MgSO4), filtered, evaporated to dryness and purified by column chromatography (SiO2; EtOAc/PE80-100° C.=1:10) to yield 4.39 g (66%) as yellow oil. MS (direct; Cl): 265 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07741352B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-608f69a0b7be4c06a95c0fdcf4ccd517 |
| Quellennotiz | uspto-grants-2010_06 |