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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 399612Erstellt: 25. Oktober 2026

4-Methoxybenzyl alcohol → 4-Methoxybenzaldehyde

https://huagongshe.com/reaction/399612

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Methoxybenzyl alcoholHCID 7738—
Edukt1,3-Dichloro-5,5-dimethylhydantoinHCID 8360—
Edukt4-ChloroanisoleHCID 12167—
EduktSodium AcetateHCID 517045—
KatalysatorTempoHCID 2724126—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-MethoxybenzaldehydeHCID 3124491,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

5 g (36.2 mmol) of anisyl alcohol, 3.0 g (36.6 mmol) of sodium acetate and 4.2 g (21.3 mmol) of dichlorodimethylhydantoin were suspended in 40 ml of methylene chloride in a 100 ml sulphonation flask. The suspension was cooled to 0° C. while stirring and treated with 10 mg (0.06 mmol) of TEMPO, whereupon the mixture was held at 0° C. for 16 hours. Thereafter, the reaction had finished without 4-chloro-anisole being formed in any amount worth mentioning. The white precipitate was filtered off and the filtrate was washed with sodium bicarbonate solution and with sodium chloride solution. Distillation of the crude product gave 4.49 g (91%) of anisaldehyde GC content: 88.8% (area percent).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05821374
Quelldatensatzuspto-grants-1998_10
ORD IDord-7fb77186813d48168788ca19dfc8ce42
Quellennotizuspto-grants-1998_10