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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77658Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/77658

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 numberUS08841326B2
Source datasetuspto-grants-2014_09
ORD IDord-c9985af20dab4ee99bc1dd8b010eb9cc
Source noteuspto-grants-2014_09