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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399612Generated: October 26, 2026

4-Methoxybenzyl alcohol → 4-Methoxybenzaldehyde

https://huagongshe.com/reaction/399612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl alcoholHCID 7738—
Reactant1,3-Dichloro-5,5-dimethylhydantoinHCID 8360—
Reactant4-ChloroanisoleHCID 12167—
ReactantSodium AcetateHCID 517045—
CatalystTempoHCID 2724126—
SolventDichloromethaneHCID 6344—
Product4-MethoxybenzaldehydeHCID 3124491.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05821374
Source datasetuspto-grants-1998_10
ORD IDord-7fb77186813d48168788ca19dfc8ce42
Source noteuspto-grants-1998_10