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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415515Generated: October 31, 2026

Benzaldehyde → 2-Phenyl-1,3-dithiane

https://huagongshe.com/reaction/2415515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBoron trifluoride etherateHCID 8000—
Reactant1,3-PropanedithiolHCID 8013—
SolventDichloromethaneHCID 6344—
Product2-Phenyl-1,3-dithianeHCID 2154787%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818787B2
Source datasetuspto-grants-2004_11
ORD IDord-d43a89cc4c8f47cd90126588163c7d29
Source noteuspto-grants-2004_11