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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1865335Erstellt: 25. Oktober 2026

Acetone → 4-(2,3-Dihydroxypropoxy)benzaldehyde

https://huagongshe.com/reaction/1865335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktMethyl morpholine oxideHCID 82029—
Edukt4-(Allyloxy)benzaldehydeHCID 95942—
KatalysatorOsmium TetroxideHCID 30318—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-(2,3-Dihydroxypropoxy)benzaldehydeHCID 16655848—

Reaktionsschritte

To a solution of 4-allyloxybenzaldehyde (1.0 g, 6.17 mmol) in acetone (40 mL) and water (5 mL) is added a 2.5% solution of OsO4 in tert. butanol (1.25 mL) followed by N-methyl morpholine-N-oxide (867 mg, 7.4 mmol). The pale yellow solution is stirred at rt for 6 h, diluted with EA (250 mL) and washed with 10% aq. citric acid solution (100 mL) and water (2×100 mL). The washings are extracted with EA (150 mL). The combined organic extracts are concentrated and purified by column chromatography on silica gel to give the title compound (731 mg) as a turbid oil. The title compound reversibly polymerizes upon standing. LC-MS: tR=0.58 min, [M+1+CH3CN]+=238.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07626037B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-ae51f2a48889486e99bab16543a0165f
Quellennotizuspto-grants-2009_12