Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1009160Erstellt: 26. Oktober 2026

Water → 3-(Benzyloxy)cyclobutan-1-one

https://huagongshe.com/reaction/1009160

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl (methylsulfinyl)methyl sulfideHCID 99129—
Edukt(((1,3-Dibromopropan-2-yl)oxy)methyl)benzeneHCID 561824—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(Benzyloxy)cyclobutan-1-oneHCID 14932787—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

Methylsulfinyl(methylthio)methane (13 ml, 125 mmol) was dissolved in 250 ml THF and cooled to −20° C. n-Butyllithium (50 ml, 125 mmol) was added and the mixture was stirred for 3 h at −20° C. The mixture was cooled down to −78° C. and a solution of 1-((1,3-dibromopropan-2-yloxy)methyl)benzene (16.000 g, 52 mmol) was added. The reaction was stirred over night and allowed to warm up to RT. It was stirred for an additional 6 h at RT, hydrolyzed with water and extracted with EtOAc. The combined organic extracts were evaporated, dissolved in ether (50 ml) and treated with conc. HCl (10 ml) for 30 min at reflux. The mixture was neutralized with NaOH (10M) and extracted with EtOAc. The combined organic extracts were dried over MgSO4 and evaporated. Glass col. Chrom. (10-50% EtOAc in Hex) gave 3-(benzyloxy)cyclobutanone as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973047B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-62640e8f36fa48219755166f11fe779e
Quellennotizuspto-grants-2011_07