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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414643Generated: October 28, 2026

Phosphorus oxychloride → 3-(5-Methyl-3-p-fluorophenyl-furan-2-yl)acrylaldehyde

https://huagongshe.com/reaction/414643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-(Dimethylamino)-2-propenalHCID 79125—
Reactant2-Methyl-4-(4'-fluorophenyl)furanHCID 14424675—
SolventAcetonitrileHCID 6342—
Product3-(5-Methyl-3-p-fluorophenyl-furan-2-yl)acrylaldehydeHCID 5428389997%

Reaction Conditions

Temperature-23 °C

Reaction Steps

A solution of 1.1 mL (11.9 mmol) of phosphorus oxychloride in 15 mL of acetonitrile was allowed to react with 1.2 mL (11.9 mmol) of 3-dimethylaminoacrolein at -23° C. After 0.25 hour at -23° C., 1.4 g (7.9 mmol) of 2-methyl-4-(4'-fluorophenyl)furan in 10 mL of acetonitrile was added dropwise. The reaction mixture was stirred at -23° C. for 0.15 hour then at 24° C. for 2 hours. The reaction was quenched upon treatment with 20 mL of 1M NaOH and extracted three times with CHCl3. The CHCl3 layers were combined, dried (MgSO4) and concentrated under reduced pressure. Column chromatography (3:1 hexanes-diethyl ether) of the residue on silica gel produced 1.76 g (97%) of 3-(5-methyl-3-p-fluorophenyl-furan-2-yl)acrylaldehyde as a solid (m.p. 89°-90° C.), homogeneous by TLC and spectroscopic criteria; Rf 0.58 (1:1 hexanes-diethyl ether); IR (KBr) 1655, 1600, 1205, 1118, 1095 cm-1 ; 1HNMR (300 MHz, CDCl3) 9.60 (d, 1H, J=10.5 Hz), 7.41 (m, 2H), 7.27 (d, 1H, J=15 Hz), 7.18 (t, 2H, J=9.0 Hz), 6.64 (dd, 1H, J=10.5 Hz, 15 Hz), 6.32 (s, 1H), 2.42 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04792614
Source datasetuspto-grants-1988_12
ORD IDord-152dd11dbeb94ad9b549f774c94fa9c9
Source noteuspto-grants-1988_12