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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462575Generated: October 24, 2026

Benzaldehyde → 4,5-Dimethyl-2-Phenyl-1,3-Dithiolane

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Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantCyclohexaneHCID 8078—
Reactant2,3-ButanedithiolHCID 548353—
SolventWaterHCID 962—
Product4,5-Dimethyl-2-Phenyl-1,3-DithiolaneHCID 20398677—

Reaction Steps

Into a 100 ml reaction flask equipped with thermometer, reflux condenser and magnetic stirring bar and hot plate with magnetic stirring apparatus is placed 0.5 grams of para-toluenesulfonic acid, 5.0 ml cyclohexane and 6.1 grams (0.05 moles) of 2,3-butanedithiol. Over a period of 25 minutes, 5.3 grams (0.05 moles) of benzaldehyde is added to the reaction mass with stirring. The reaction mass is then heated to reflux with stirring and refluxed for a period of 9.5 hours while taking off water of reaction. At the end of the refluxing period, the reaction mass is cooled to room temperature and transferred to a separatory funnel. The reaction mass is then washed with one 50 ml portion of saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and filtered. The resulting filtrate is distilled on a Microvigreux column yielding the following three fractions:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515968
Source datasetuspto-grants-1985_05
ORD IDord-677da6f870204dd18eaecd4cabad47c2
Source noteuspto-grants-1985_05