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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714171Generated: October 25, 2026

Acetone → 1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-one

https://huagongshe.com/reaction/714171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant3-FluorobenzaldehydeHCID 68009—
SolventEthanolHCID 702—
Product1,5-Bis(3-fluorophenyl)-1,4-pentadien-3-oneHCID 6950172242%

Reaction Steps

3-Fluorobenzaldehyde (1s, 0.5 ml, 4.7 mmol) and acetone (19, 0.18 ml, 2.3 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.29 g, 7.3 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting mixture was filtered and chromatographed on silica gel with ethyl acetate/hexane to give a solid. The crude was recrystallized from ethanol to afford 0.26 g (42%) of yellow crystals: mp 96-97° C. [expected mp 96-97° C.]; 1H NMR: δ 7.03 (d, 2H, J=16.1 Hz), 7.09 (m, 2H), 7.35 (m, 6H), 7.67 (d, 2H, J=15.9 Hz); 13C NMR: δ 114.4, 117.5, 124.4, 126.3, 130.4, 136.9, 142.0, 162.9, 188.1; Anal. Calcd for C17H12OF2: C, 75.55; H, 4.48. Found: C, 75.26; H, 4.65.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187397B2
Source datasetuspto-grants-2015_11
ORD IDord-6ac76e8e1e11405c82345397eaae86a8
Source noteuspto-grants-2015_11