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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 568980Erstellt: 25. Oktober 2026

Dimethyl Sulfoxide → 2,2-Difluoro-5-methoxy-1-pentanal hydrate

https://huagongshe.com/reaction/568980

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt2,2-Difluoro-5-methoxypentan-1-olHCID 14097599—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,2-Difluoro-5-methoxy-1-pentanal hydrateHCID 2014945353,4%

Reaktionsbedingungen

Temperatur-60 °C

Reaktionsschritte

A solution of dry dimethylsulfoxide (3 g, 38 mmoles) in dry dichloromethane (15 ml) is slowly added to a solution of oxalyl chloride (2.4 g, 19 mmoles) in dichloromethane (15 ml), kept under nitrogen and cooled to -60° C. Stirring is continued for 15 min. at -60° C. and followed by addition of 2,2-difluoro-1-hydroxy-5-methoxypentane (2.7 g, 17.5 mmoles) in dichloromethane (15 ml). The reaction mixture is stirred for 11/2 hours at -60° C., triethylamine (8.4 ml, 114 mmoles) in dichloromethane (15 ml) is slowly added, and the cooling bath is removed. The reaction mixture is hydrolyzed with brine and diluted with dichloromethane. The organic phase is then washed successively with 2N HCl containing some sodium chloride, and brine. Usual work-up affords the title compound (1.59 g, 53%) which is used for the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04730006
Quelldatensatzuspto-grants-1988_03
ORD IDord-7857d77b235a47458505ec6d65fe4927
Quellennotizuspto-grants-1988_03