Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646580Generated: October 25, 2026

Phenylacetaldehyde → 2-Benzyl-1,3-dithiane

https://huagongshe.com/reaction/1646580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetaldehydeHCID 998—
ReactantBoron trifluoride etherateHCID 8000—
Reactant1,3-PropanedithiolHCID 8013—
ReactantPotassium HydroxideHCID 14797—
SolventDichloromethaneHCID 6344—
Product2-Benzyl-1,3-dithianeHCID 30029191%

Reaction Steps

To a solution of 33.9 g (280 mmol) of phenylacetaldehyde and 35.6 g (330 mmol) of 1,3-propanedithiol in 300 mL of methylene chloride at 0° C., was added, dropwise over a period of 30 minutes, 10 mL of boron trifluoride etherate. The reaction mixture was allowed to warm to ambient temperature and stirred for 3 h at ambient temperature. The reaction mixture was made basic by the addition of 180 mL of 5% aqueous potassium hydroxide solution and the resultant mixture was stirred for 0.5 h. The layers were separated and the aqueous layer was extracted with methylene chloride. The combined organic extract was washed with 1N aqueous sodium hydroxide solution and brine, dried over anhydrous magnesium sulfate, filtered and the filtrate was distilled to afford 53.62 g (91% yield) of the title compound, b.p. 150° C. (2 mm Hg); 1H NMR (CDCl3) δ1.75-1.95 (1H, m), 2.05-2.17 (1H, m), 2.75-2.91 (4H, m), 3.03 (2H, d, J=9 Hz), 4.25 (1H, t, J=9 Hz), 7.17-7.38 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180733
Source datasetuspto-grants-1993_01
ORD IDord-2b9fd1d276aa4a9cbdfac5a9fefc4f71
Source noteuspto-grants-1993_01