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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1275911Erstellt: 26. Oktober 2026

Dimethylformamide → (3-Ethylphenyl)methanol

https://huagongshe.com/reaction/1275911

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktBenzene, 1-bromo-3-ethyl-HCID 123170—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(3-Ethylphenyl)methanolHCID 104659—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

n-Butyllithium (34 ml of a 2.5M solution in hexanes) was added to a solution of 1-bromo-3-ethylbenzene (15 g) in tetrahydrofuran at -78° C. After 1 hour dimethylformamide (15 ml) was added. The mixture was stirred at -78° C. for 1 hour and allowed to warm to room temperature. The mixture was quenched with aqueous ammonium chloride and partitioned between ethyl acetate and water. The organic phase was dried (MgSO4) and evaporated. The residue was dissolved in methanol (250 ml) and treated with sodium borohydride (1.51 g) portionwise. The mixture was stirred at room temperature for 16 hours, quenched with 2M HCl (100 ml) and stirred for 4 hours. The mixture was concentrated under reduced pressure and the residue partitioned between ethyl acetate and 2M HCl. The organic phase was dried (MgSO4), evaporated and the residue purified by chromatography eluting with 5-10% ethyl acetate in isohexane. Yield 7.6 g.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06162808
Quelldatensatzuspto-grants-2000_12
ORD IDord-9bf85f2a6660443180bd43c78a3d6f42
Quellennotizuspto-grants-2000_12