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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1391781Erstellt: 26. Oktober 2026

Tetrahydrofuran → Ethyl 3-(4-Hydroxy-3,5-Dimethoxyphenyl)Acrylate

https://huagongshe.com/reaction/1391781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktSyringaldehydeHCID 8655—
EduktP-ToluenesulfonylhydrazideHCID 15303—
EduktSodium hydrideHCID 24758—
ProduktEthyl 3-(4-Hydroxy-3,5-Dimethoxyphenyl)AcrylateHCID 6439771—

Reaktionsschritte

To a stirred solution of triethyl phosphonoacetate (0.60 mL, 3.02 mmol) in THF (5 mL) was added portion-wise NaH (60% dispersion in mineral oil, 360 mg, 9.00 mmol) over 2-3 mins. After effervescence had ceased, 4-hydroxy-3,5-dimethoxybenzaldehyde (547 mg, 3.00 mmol) was added portion-wise, washing in with THF (3 mL). More THF (2×2 mL) was added to the thick slurry and the resulting mixture was then heated to reflux for 21 hours. The mixture was then allowed to cool slowly to ambient temperature and the reaction quenched by the careful addition of saturated aqueous NH4Cl (20 mL). The organic solvent was then removed under vacuum and the resulting aqueous mixture was then extracted with DCM (10 mL, 5 mL and then 2 mL) using hydrophobic frits. The filtrate was then treated with Polymer Supported-TsNHNH2 resin (loading 3.22 mmol/g, 1.62 g, 5.23 mmol (3 eq wrt unreacted aldehyde)) and the mixture stirred for 16 hours to remove any unreacted aldehyde. The resin was then removed by filtration washing with DCM (5 mL, 10 mL and then 5 mL) and the filtrate reduced under vacuum to give the title compound (221 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07338960B2
Quelldatensatzuspto-grants-2008_03
ORD IDord-98ffb6f561f64b1982844057862db2a3
Quellennotizuspto-grants-2008_03