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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888544Generated: October 26, 2026

Hydrochloric Acid → Methyl 6,6-dimethyl-5-trifluoromethyl-2-(3,3,3-trifluoropropylsulfonyl)heptanoate

https://huagongshe.com/reaction/888544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(3,3,3-trifluoropropylsulfonyl)acetateHCID 57425720—
Reactant4,4-Dimethyl-3-(trifluoromethyl)pentyl p-toluenesulfonateHCID 59378432—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl 6,6-dimethyl-5-trifluoromethyl-2-(3,3,3-trifluoropropylsulfonyl)heptanoateHCID 5937845058.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 2.9 g of 4,4-dimethyl-3-(trifluoromethyl)pentyl p-toluenesulfonate and 2.0 g of methyl (3,3,3-trifluoropropylsulfonyl)acetate in 30 ml of dimethyl sulfoxide was added 1.2 g of potassium carbonate at room temperature. The reaction mixture was heated to 90° C., stirred at the same temperature for 6 hours, and then 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 2.00 g of methyl 6,6-dimethyl-5-trifluoromethyl-2-(3,3,3-trifluoropropylsulfonyl)heptanoate (hereinafter referred to as the present compound (7)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247612B2
Source datasetuspto-grants-2012_08
ORD IDord-59c15ecbba334c7e9ec4a4461e58111e
Source noteuspto-grants-2012_08