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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493829Generated: October 26, 2026

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

https://huagongshe.com/reaction/1493829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantChlorosuccinimideHCID 31398—
Reactant3,7,11-Trimethyl-2,6,10-tridecatrien-1-olHCID 53916694—
SolventDichloromethaneHCID 6344—
Product1-Chloro-3,7,11-trimethyldodeca-2,6,10-trieneHCID 407340985%

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 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025003
Source datasetuspto-grants-1991_06
ORD IDord-0802f604dc1949b29215f2317daf5778
Source noteuspto-grants-1991_06