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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327903Generated: October 26, 2026

Dimethyl Sulfide → (E,E)-Farnesyl chloride

https://huagongshe.com/reaction/327903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantChlorosuccinimideHCID 31398—
Reactant(E,E)-3,7,11-trimethyl-2,6,10-tridecatrien-1-olHCID 86746852—
SolventDichloromethaneHCID 6344—
Product(E,E)-Farnesyl chlorideHCID 600339785%

Reaction Conditions

Temperature0 °C

Reaction Steps

(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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273969
Source datasetuspto-grants-1993_12
ORD IDord-b3ec51d10dd941a0a6113016e7dafb45
Source noteuspto-grants-1993_12