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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1646580Erstellt: 25. Oktober 2026

Phenylacetaldehyde → 2-Benzyl-1,3-dithiane

https://huagongshe.com/reaction/1646580

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylacetaldehydeHCID 998—
EduktBoron trifluoride etherateHCID 8000—
Edukt1,3-PropanedithiolHCID 8013—
EduktPotassium HydroxideHCID 14797—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Benzyl-1,3-dithianeHCID 30029191%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05180733
Quelldatensatzuspto-grants-1993_01
ORD IDord-2b9fd1d276aa4a9cbdfac5a9fefc4f71
Quellennotizuspto-grants-1993_01