Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249129Erstellt: 24. Oktober 2026

Dimethyl Sulfide → (E,E)-Farnesyl chloride

https://huagongshe.com/de/reaction/249129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfideHCID 1068—
EduktChlorosuccinimideHCID 31398—
Edukt(E,E)-3,7,11-trimethyl-2,6,10-tridecatrien-1-olHCID 86746852—
LösungsmittelDichloromethaneHCID 6344—
Produkt(E,E)-Farnesyl chlorideHCID 6003397—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

(Note: all temperatures indicated are for the contents of the reaction flask). To a stirred solution of 299 mg (2.24 mmol) of N-chlorosuccinimide in 15 ml of dichloromethane at -30° C. under argon was added 0.18 ml (2.45 mmol) of distilled dimethyl sulfide over 5 minutes. After 10 minutes at -30° C., the reaction was allowed to warm to 0° C. for 10 minutes, followed by cooling to -40° C. A solution of 441.4 mg (1.99 mmol) of (E,E)-3,7,11-trimethyl-2,6,10-tridecatrien-1-ol in 5 ml of dichloromethane was added dropwise over 10 minutes. The reaction was allowed to warm gradually to 0° C. over 1 hour, and then maintained at 0° C. for 1 hour. After quenching with cold water, the mixture was extracted with hexane and the hexane extract was washed with cold water and cold brine, dried (MgSO4) and evaporated to afford 483 mg of a crude product. Rapid flash chromatography on 20 g of Merck 9385 silica gel eluted with 3:97 ethyl acetate:pet ether provided 406.5 mg 85%) of a colorless liquid. 13C NMR indicated that this material contained a trace (3%) impurity.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05212164
Quelldatensatzuspto-grants-1993_05
ORD IDord-aa171c7a5c474f2a804ca7e31808e167
Quellennotizuspto-grants-1993_05