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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 529865Generated: October 31, 2026

1-Pentanol → Triphenylsulfonium 2,4,6-triisopropylbenzoate

https://huagongshe.com/reaction/529865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PentanolHCID 6276—
Reactant3-Methyl-2-butanoneHCID 11251—
ReactantTriphenylsulfonium methylsulfateHCID 22995011—
ReactantSodium 2,4,6-triisopropylbenzoateHCID 118556701—
SolventWaterHCID 962—
ProductTriphenylsulfonium 2,4,6-triisopropylbenzoateHCID 13173563180%

Reaction Steps

A 1-L eggplant shaped flask was charged with 22.4 g of sodium 2,4,6-triisopropylbenzoate (prepared in Synthesis Example 1-2), 31.1 g of triphenylsulfonium methylsulfate, 90 g of methyl isopropyl ketone, 90 g of 1-pentanol, and 40 g of water, which were stirred at room temperature for 1 hour. The organic layer was separated from the reaction mixture and washed with water. After washing, the organic layer was concentrated by distilling off the solvent. The liquid concentrate was crystallized from 300 g of diisopropyl ether. The crystal precipitate was filtered and dried, obtaining the target compound, triphenylsulfonium 2,4,6-triisopropylbenzoate as white crystal. Amount 40.4 g, yield 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09348227B2
Source datasetuspto-grants-2016_05
ORD IDord-c896c67c342f48fa8f84747cf3535aa3
Source noteuspto-grants-2016_05