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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324456Erstellt: 24. Oktober 2026

Dimethylformamide → (3-Ethylphenyl)methanol

https://huagongshe.com/de/reaction/324456

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 (320 ml) at −78° C. After 1 hour N,N-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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218376B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-7614c6145c424c9396a8ab177d39f1fb
Quellennotizuspto-grants-2001_04