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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20053Erstellt: 24. Oktober 2026

Water → 3-(Benzyloxy)cyclobutan-1-one

https://huagongshe.com/de/reaction/20053

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt(((1,3-Dibromopropan-2-yl)oxy)methyl)benzeneHCID 561824—
Edukt3-(Benzyloxy)cyclobutanone Methylsulfinyl(methylthio)methaneHCID 86614138—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(Benzyloxy)cyclobutan-1-oneHCID 14932787—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

3-(Benzyloxy)cyclobutanone 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 6h 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
PatentnummerUS07745484B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-209392541b7d4708aa42d3647a0d987d
Quellennotizuspto-grants-2010_06