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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 445819Erstellt: 24. Oktober 2026

Sodium hydride → (E)-4-(4-methoxyphenyl)but-3-enoic acid

https://huagongshe.com/de/reaction/445819

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt4-MethoxybenzaldehydeHCID 31244—
Edukt(2-Carboxyethyl)triphenylphosphonium bromideHCID 2733850—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(E)-4-(4-methoxyphenyl)but-3-enoic acidHCID 1471304955,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The mixture of (2-carboxyethyl)triphenylphosphonium bromide (20.0 g, 54.0 mmol) and 4-methoxybenzaldehyde (6.5 g, 53.5 mmol) in anhydrous DMSO (64 mL) was added slowly to the suspension of 60% NaH in mineral oil (4.3 g, 107 mmol) in anhydrous tetrahydrofuran (32 mL). The reaction mixture was stirred at 0° C. for 30 minutes then warmed to room temperature over 4 hours. The reaction mixture was quenched with 1N HCl (150 mL) and extracted with ethyl acetate. The organic phase was washed with water, brine, dried with sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (50% EtOAc in hexanes) to provide (E)-4-(4-methoxyphenyl)but-3-enoic acid (557) (5.7 g, 55.0%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476308B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-acebfbeec9024465921b93a880490b57
Quellennotizuspto-grants-2013_07