Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888334Generated: October 25, 2026

Hydrochloric Acid → 6-Methyl-2-(3,3,3-trifluoropropylsulfonyl)-7-octynenitrile

https://huagongshe.com/reaction/888334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(3,3,3-Trifluoropropylsulfonyl)acetonitrileHCID 57425671—
Reactant4-Methyl-5-hexynyl methanesulfonateHCID 59378474—
SolventDimethyl SulfoxideHCID 679—
Product6-Methyl-2-(3,3,3-trifluoropropylsulfonyl)-7-octynenitrileHCID 8664298729%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1.0 g of 4-methyl-5-hexynyl methanesulfonate and 1.1 g of (3,3,3-trifluoropropylsulfonyl)acetonitrile in 30 ml of dimethyl sulfoxide was added 0.7 g of potassium carbonate at room temperature. The reaction mixture was stirred at 60° C. for 2 days. The reaction mixture was allowed to stand to cool to nearly room temperature. To the reaction mixture was added 10% hydrochloric acid and then extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography to obtain 0.45 g of 6-methyl-2-(3,3,3-trifluoropropylsulfonyl)-7-octynenitrile (hereinafter referred to as the present compound (28)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247595B2
Source datasetuspto-grants-2012_08
ORD IDord-15d67979df5441e292fb499fbfecbcaf
Source noteuspto-grants-2012_08