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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 470605Erstellt: 26. Oktober 2026

Sodium hydride → HCID 136413210, Verbindung

https://huagongshe.com/reaction/470605

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic Acid Methyl EsterHCID 67396155—
EduktHCID 178449909HCID 178449909—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 136413210HCID 136413210—

Reaktionsschritte

A solution of N-hydroxy-butyramidine (0.24 g, 2.34 mmol) in tetrahydrofuran (5 mL) was added slowly into the suspension of 60% sodium hydride (0.14 g, 3.5 mmol) in dry tetrahydrofuran (5 mL) under nitrogen atmosphere at 0° C. to 10° C. The mixture was stirred for 30 min at room temperature. 3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic acid methyl ester (compound of Example 1, Step 1; 0.5 g, 1.18 mmol) in dry tetrahydrofuran (5 mL) was added into the reaction mixture and heated at 60° C. for 8 h. The reaction mixture was cooled at 0° C. and quenched with methanol (2 mL) to destroy excess sodium hydride. The reaction mixture was extracted with ethyl acetate (2×10 mL) and the combined organic layers were washed with water (2×10 mL) followed by brine (10 mL). The organic phase obtained was dried over anhydrous sodium sulphate and concentrated to dryness. The crude product obtained was purified by column chromatography (silica gel, chloroform-methanol) to afford the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629277B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-4c664d48321d4babab4ca34308e1347e
Quellennotizuspto-grants-2014_01