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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265300Generated: November 1, 2026

Phenylacetaldehyde → 2-Benzyl-1,3-oxathiane

https://huagongshe.com/reaction/265300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetaldehydeHCID 998—
Reactantp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
Product2-Benzyl-1,3-oxathianeHCID 12395918—

Reaction Steps

To a solution of the thiol (14.67 g) from step a) in toluene (200 ml) was added p-toluenesulphonic acid (1 g) and phenylacetaldehyde (18.3 ml). The reaction was refluxed using a Dean and Stark apparatus. After the appropriate amount of water had been collected the reaction mixture was cooled, washed with saturated sodium bicarbonate, saturated brine and dried (K2CO3). The crude product was distilled (bp 100°-110°/0.3 mbars) to give a yellow liquid (19.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648370
Source datasetuspto-grants-1997_07
ORD IDord-5425f26ac9104f96946daa35a5859e89
Source noteuspto-grants-1997_07