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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273343Erstellt: 25. Oktober 2026

3,4,5-Trimethoxybenzaldehyde → 1-(3,4,5-Trimethoxyphenyl)-2-propyn-1-ol

https://huagongshe.com/reaction/273343

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,4,5-TrimethoxybenzaldehydeHCID 6858—
EduktHCID 178463197HCID 178463197—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(3,4,5-Trimethoxyphenyl)-2-propyn-1-olHCID 1611032773,3%

Reaktionsschritte

A solution of 3,4,5-trimethoxybenzaldehyde (1.0 g, 5.0 mmol) in THF (50 mL) was stirred at 0° C. Sodium acetylide (18% w.t. slurry in xylene, 1.63 g, 6.1 mmol) was added via syringe. The reaction mixture was stirred overnight at room temperature and quenched by water. It was then extracted with EtOAc (30 mL×3). The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered, and concentrated to give a crude product, which was purified by flash column chromatography eluting with EtOAc/n-hexane (1:2) to afford 1-(3,4,5-trimethoxyphenyl)prop-2-yn-1-ol as a white solid (815 mg, 72%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456289B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-706fa45e5dde4051bca2c44091994724
Quellennotizuspto-grants-2008_11