Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850429Generated: October 26, 2026

Dimethyl Sulfoxide → 3-Methoxy-2-(pentyloxy)benzaldehyde

https://huagongshe.com/reaction/850429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
Reactant(3-Methoxy-2-pentyloxyphenyl)methanolHCID 19363470—
SolventWaterHCID 962—
Product3-Methoxy-2-(pentyloxy)benzaldehydeHCID 1936329097.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

The crude product of (3-methoxy-2-pentyloxyphenyl)methanol (1.2 g), dimethyl sulfoxide (DMSO, 25 ml) and triethylamine (6.72 ml, 48.2 mmol) were mixed, and this solution was cooled to 0° C. Sulfur trioxide--pyridine complex (2.56 g, 16.1 mmol) was added, and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into water to stop the reaction, and the aqueous layer was extracted 3 times with ethyl acetate (30 ml). The organic layers were combined, washed with 2N hydrochloric acid (30 ml), water (30 ml) and saturated brine (30 ml), and dried over anhydrous magnesium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography (hexane/ethyl acetate=15/1-10/1) to give 3-methoxy-2-pentyloxybenzaldehyde (1.16 g, 83% in 3 steps) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-4619f26ca0ab42a5809218a8b39a7def
Source noteuspto-grants-2000_01