HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Chloride → Coniferyl ferulate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Chloride | HCID 312 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-Acetoxyconiferyl alcohol | HCID 131737178 | — |
| Edukt | 4-Acetoxyferuloyl chloride | HCID 131737179 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Chloroform ethylacetate | HCID 21584013 | — |
| Produkt | Acetoacetic Acid | HCID 96 | — |
| Produkt | Coniferyl ferulate | HCID 6441913 | 94% |
Reaktionsschritte
Coupling of 4-acetoxyferuloyloyl chloride with 4-acetoxyconiferyl alcohol was efficiently carried out using 4-(dimethylamino)-pyridine (DMAP). Thus, 4-acetoxyconiferyl alcohol and 4-acetoxyferuloyl chloride were dissolved in dry CH2Cl2 (120 mL) to which DMAP (0.25 equiv) and Et3N (0.85 equiv) were added. The mixture was stiffed for 2 h, when TLC [CHCl3/EtOAc (5:1)] showed the starting material was converted into a faster moving compound. The solution was diluted with CH2Cl2 and washed successively with aqueous 3% HCl and saturated NH4Cl. Drying over MgSO4, evaporation, and purification by flash chromatography [CHCl3/EtOAc (19:1)] gave the diacetate of coniferyl ferulate (94%) as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09441235B2 |
| Quelldatensatz | uspto-grants-2016_09 |
| ORD ID | ord-1c29e8ee799c46e9b7cd1445aa3b90f7 |
| Quellennotiz | uspto-grants-2016_09 |