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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 880Erstellt: 23. Oktober 2026

3-Phenoxybenzyl alcohol → 3-Phenoxybenzaldehyde

https://huagongshe.com/de/reaction/880

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Phenoxybenzyl alcoholHCID 26295—
KatalysatorManganese dioxideHCID 14801—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-PhenoxybenzaldehydeHCID 3828490,1%

Reaktionsschritte

To a solution of 1.8mL (10.3 mmol) of 3-phenoxybenzyl alcohol (Aldrich Chemical Co.) in 20 mL of CH2Cl2 at room temperature was added 1.5 g of powdered 4 Å molecular sieves and 2.5 g of activated MnO2. The resulting suspension was stirred at room temperature for 0.5 h, at which time an additional 2.5 g of MnO2 was added. After stirring at room temperature for 0.5 h the reaction mixture was filtered through celite to give 1.84 g of the aldehyde 125 as an oil. 1H NMR consistent with structure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723459
Quelldatensatzuspto-grants-1998_03
ORD IDord-1489d72d83a3432b8980d4f94eed3de6
Quellennotizuspto-grants-1998_03