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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231115Generated: November 3, 2026

Dimethyl Sulfoxide → 4-Methoxy-3,5-dimethylbenzaldehyde

https://huagongshe.com/reaction/2231115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 2758574HCID 2758574—
SolventDichloromethaneHCID 6344—
Product4-Methoxy-3,5-dimethylbenzaldehydeHCID 275857394.7%

Reaction Steps

The aldehyde was synthesized according to the procedure of Example 46, Step 1 using the alcohol from Step 2 (7.5 g, 45 mmol), oxalyl chloride (6.35 g, 50 mmol), dimethylsulfoxide (8.8 g, 100 mmol) and triethylamine (10.2 g, 110 mmol) and in methylene chloride (100 ml). There was obtained 7 g (92%) of the desired aldehyde which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06426360B1
Source datasetuspto-grants-2002_07
ORD IDord-e0086035a1674424834efe0944aee7f0
Source noteuspto-grants-2002_07