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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 465754Erstellt: 24. Oktober 2026

Methanol → 2-Benzoyloxy-4-hydroxymethylcyclobutanone

https://huagongshe.com/de/reaction/465754

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktDichloromethaneHCID 6344—
Edukt1-Benzoyloxy-3-hydroxymethyl-2-methylenecyclobutaneHCID 19794316—
Produkt2-Benzoyloxy-4-hydroxymethylcyclobutanoneHCID 1979431886%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A mixture of 2.09 g (9.5 mmol) of 1-benzoyloxy-3-hydroxymethyl-2-methylenecyclobutane from Step G, 112 mL of methylene chloride and 28 mL of methanol was cooled to -78° C. under a nitrogen atmosphere. Ozone was bubbled through the mixture for 10 minutes, until a persistent blue color was observed. Excess ozone was flushed out with nitrogen, 9 mL of dimethyl sulfide was added and the reaction mixture stirred for 0.5 h at -78° C. The reaction mixture was allowed to warm to ambient temperature, stirred for 0.5 h at ambient temperature and evaporated under reduced pressure to a syrup. The syrup (2.5 g) was dissolved to ~2 mL of methylene chloride and purified on a 1.5×45 cm silica gel column eluted @5 psi with 100 mL of methylene chloride, followed by 250 mL of 1% methanol in methylene chloride and 250 mL of 2% methanol in methylene chloride to give 1.79 g (86% yield) of the title compound; MS DCI-NH3M/Z: 221 (M+H)+, 238 (M+NH4)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05153352
Quelldatensatzuspto-grants-1992_10
ORD IDord-1feec820aa13497abe34e4a1104358fe
Quellennotizuspto-grants-1992_10