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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56765Generated: October 25, 2026

p-Toluenesulfonic acid → 1,3-Dithiane-2-carboxylic acid

https://huagongshe.com/reaction/56765

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1,3-PropanedithiolHCID 8013—
ReactantGlyoxylic acid, monohydrateHCID 15620607—
SolventTolueneHCID 1140—
Product1,3-Dithiane-2-carboxylic acidHCID 303705—

Reaction Steps

9.20 g (100 mmol) of glyoxalic acid monohydrate, 11.1 ml (110 mmol) of 1,3-propanedithiol and 1.72 g (10.0 mmol) of para-toluenesulphonic acid were heated in 200 ml of toluene under reflux for 3 h. The reaction mixture was cooled to RT and extracted three times with 100 ml of saturated aqueous sodium bicarbonate solution. The combined aqueous phases were washed with 200 ml of diethyl ether, acidified with aqueous hydrochloric acid (6N) and extracted four times with 200 ml of ethyl acetate. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The residue was used for the next step without further purification. Yield: 8.0 g (47% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434690B2
Source datasetuspto-grants-2016_09
ORD IDord-44198022921e4074961d14a1761bdab7
Source noteuspto-grants-2016_09