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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 61510Erstellt: 25. Oktober 2026

Chloride → Coniferyl ferulate

https://huagongshe.com/reaction/61510

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorideHCID 312—
EduktTriethylamineHCID 8471—
Edukt4-Acetoxyconiferyl alcoholHCID 131737178—
Edukt4-Acetoxyferuloyl chlorideHCID 131737179—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelChloroform ethylacetateHCID 21584013—
ProduktAcetoacetic AcidHCID 96—
ProduktConiferyl ferulateHCID 644191394%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09441235B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-1c29e8ee799c46e9b7cd1445aa3b90f7
Quellennotizuspto-grants-2016_09