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HRID 374269Erstellt: 24. Oktober 2026

Dimethyl Sulfide → 1-Chloro-3,7,11-trimethyldodeca-2,6,10-triene

https://huagongshe.com/de/reaction/374269

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfideHCID 1068—
EduktChlorosuccinimideHCID 31398—
EduktHCID 53916694HCID 53916694—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Chloro-3,7,11-trimethyldodeca-2,6,10-trieneHCID 407340985%

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 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:petroleum 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
PatentnummerUS05166386
Quelldatensatzuspto-grants-1992_11
ORD IDord-e862876f0adf45c28fec08c4415f3561
Quellennotizuspto-grants-1992_11