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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 254855Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/254855

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 it 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
PatentnummerUS07875726B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-c7cd5571193440c9b7466399a660232c
Quellennotizuspto-grants-2011_01