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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 552278Erstellt: 26. Oktober 2026

3,5-Dimethyl-4-hydroxybenzaldehyde → 3-(4-Hydroxy-3,5-dimethyl-phenyl)-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-one

https://huagongshe.com/reaction/552278

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-Dimethyl-4-hydroxybenzaldehydeHCID 75222—
Edukt1-(5-Ethyl-4-phenyl-thiophen-2-yl)-ethanoneHCID 67166164—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
Produkt3-(4-Hydroxy-3,5-dimethyl-phenyl)-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-oneHCID 5924898858,2%

Reaktionsschritte

A solution of 1-(5-ethyl-4-phenyl-thiophen-2-yl)-ethanone (64 mg, 0.278 mmol) and 3,5-dimethyl-4-hydroxybenzaldehyde (53 mg, 0.334 mmol) in ethanol (1.2 mL) and 5 N HCl in isopropanol (0.6 mL) is stirred at rt for 1 h. The dark green solution is diluted with water and extracted with EA. The organic extract is evaporated, dissolved in methanol (1 mL) and THF (1 mL), and treated with Pd/C (60 mg, 10% Pd). The slurry is hydrogenated under 1.4 bar of H2 for 1.5 h. The mixture is filtered over celite, the solvent is removed in vacuo and the crude product is purified on prep. TLC plates with heptane:EA 2:1 to give 3-(4-hydroxy-3,5-dimethyl-phenyl)-1-(5-ethyl-4-phenyl-thiophen-2-yl)-propan-1-one (59 mg) as a yellow oil; LC-MS: tR=1.11 min; 1H NMR (CDCl3): δ 7.58 (s, 1H), 7.46-7.30 (m, 5H), 6.85 (s, 2H), 4.56 (s, 1H), 3.18-3.10 (m, 2H), 2.97-2.86 (m, 4H), 2.22 (s, 6H), 1.30 (t, J=7.6 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07951794B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-f9f4bea4cd2141c78ebf498dcad1bca1
Quellennotizuspto-grants-2011_05