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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766955Generated: November 1, 2026

Trifluoroacetic acid → p-Toluenesulfonic acid

https://huagongshe.com/reaction/1766955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productp-Toluenesulfonic acidHCID 6101—

Reaction Steps

Ten (10) g of Boc-(13C-Leu)-OH.H2O was dissolved in ethanol (50 ml)-water (20 ml) and 6.52 g of cesium carbonate dissolved in 20 ml of distilled water was added. After concentration under reduced pressure, ethanol and toluene were added and the remaining water was azeotropically removed out to yield a gel product, which was suspended in 300 ml of DMF. To the suspension, 5.2 ml of benzyl bromide was added dropwise at room temperature while being stirred. After stirring at room temperature for 45 minutes, the solvent was distilled out under reduced pressure. Ethyl acetate was added and washed with water. After drying over anhydrous sodium sulfate, ethyl acetate was distilled out under reduced pressure to yield an oily product. To the product, 59 ml of TFA was added and stirred at room temperature for 40 minutes. After adding 8.37 g of p-toluenesulfonic acid monohydrate, TFA was distilled out under reduced pressure. Diisopropyl ether was added to the residue to crystallize to yield TosOH.H-(13C-Leu)-OBzl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232559B1
Source datasetuspto-grants-2007_06
ORD IDord-cce4fe3067bf402d9d06bd9b737ea0d9
Source noteuspto-grants-2007_06