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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384539Erstellt: 24. Oktober 2026

Benzaldehyde → 2-Phenyl-1,3-dithiane

https://huagongshe.com/de/reaction/384539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktBoron trifluoride etherateHCID 8000—
Edukt1,3-PropanedithiolHCID 8013—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Phenyl-1,3-dithianeHCID 2154787%

Reaktionsschritte

To a solution of benzaldehyde (10.6 g, 100 mmol) and 1,3-propane dithiol in CH2Cl2 (150 mL) at room temperature was dropwise added BF3.Et2O (6.3 mL, 50 mmol) and the resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was then diluted with CH2Cl2, filtered and the filtrate washed with brine, saturated NaHCO3, brine and dried over Na2SO4. The solvent was removed under reduced pressure to afford a white solid, which was recrystallized from a 1:1 mixture of ether and hexane to afford 17.0 g (87%) of the title compound (65) as white crystalline needles. 1H NMR (CDCl3, 400 MHz): δ 1.91 (m, 1H), 2.14 (m, 1H), 2.89 (m, 2H), 3.04 (m, 2H), 5.16 (s, 1H), 7.35-7.28 (m, 3H), 7.46 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367722B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-f472770636b44d42a59342f290c22ba6
Quellennotizuspto-grants-2013_02