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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714173Generated: October 26, 2026

Acetone → 1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-one

https://huagongshe.com/reaction/714173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactanto-(Trifluoromethyl)benzaldehydeHCID 123067—
SolventEthanolHCID 702—
Product1,5-Bis(2-trifluoromethylphenyl)-1,4-pentadien-3-oneHCID 8543407988.7%

Reaction Steps

2-(Trifluoromethyl)-benzaldehyde (1w, 0.75 ml, 5.7 mmol) and acetone (19, 0.21 ml, 2.8 mmol) were combined in ethanol (20 ml) and stirred for 10 min at room temperature. A solution of sodium hydroxide (0.34 g, 8.5 mmol) and water (15 ml) was added and the mixture stirred for 18 hr at room temperature. The resulting precipitate was filtered and recrystallized from ethanol to afford 0.92 g (87%) of a yellow solid: mp 131-133° C. [expected mp 131° C.]; 1H NMR: δ 6.99 (d, 2H, J=15.9 Hz), 7.48 (t, 2H, J=7.6 Hz), 7.56 (t, 2H, J=7.0 Hz), 7.70 (d, 2H, J=7.7 Hz), 7.77 (d, 2H, J=7.6 Hz), 8.07 (d, 2H, J=15.7 Hz); 13C NMR: δ 123.9, 126.2, 127.9, 128.8, 129.4, 129.7, 132.1, 133.7, 139.1, 188.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187397B2
Source datasetuspto-grants-2015_11
ORD IDord-4da9f86573cc4d1ba9c30cdb355a2b03
Source noteuspto-grants-2015_11