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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888329Generated: October 31, 2026

Hydrochloric Acid → HCID 86642983, compound

https://huagongshe.com/reaction/888329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-1-hexeneHCID 75906—
ReactantMethyl 2-(3,3,3-trifluoropropylsulfonyl)acetateHCID 57425720—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86642983HCID 8664298379.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 2.0 g of 6-bromo-1-hexene and 2.9 g of methyl (3,3,3-trifluoropropylsulfonyl)acetate in 50 ml of dimethyl sulfoxide, 0.5 g of sodium hydride (60% in oil) was added at room temperature. The mixture was heated to 60° C., stirred for 4 hours, and then allowed to stand near room temperature. To the reaction mixture, 10% hydrochloric acid was added, followed by extraction 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 3.10 g of methyl 2-(3,3,3-trifluoropropylsulfonyl)-7-octenoate (hereinafter referred to as the present compound (20)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247595B2
Source datasetuspto-grants-2012_08
ORD IDord-4ce8cad8df7040efb66302c0450b9e6b
Source noteuspto-grants-2012_08