Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440397Generated: October 29, 2026

Dimethyl Sulfoxide → 3-(1-Dodecyl)-5-isoxazolecarboxaldehyde

https://huagongshe.com/reaction/440397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Isoxazolemethanol, 3-dodecyl-HCID 10635553—
SolventDichloromethaneHCID 6344—
Product3-(1-Dodecyl)-5-isoxazolecarboxaldehydeHCID 1837297282.8%

Reaction Conditions

Temperature-60 °C

Reaction Steps

A solution of oxalyl chloride (28.8 ml) in dry dichloromethane (100 ml) was cooled to -60° C. and a solution of dimethylsulfoxide (8.9 ml) in dichloromethane (30 ml) was added, followed by a slurry of 3-(1-dodecyl)-5-isoxazolemethanol (14.0 g) in dry dichloromethane (200 ml). The mixture was stirred at -60° C. for 1 hr, quenched with triethylamine (87 ml) and allowed to warm to room temperature. The solution was poured into water (300 ml) and extracted with dichloromethane. The organic phases were washed with dilute citric acid solution, dried, filtered, and the filtrate was evaporated. The residue was passed through a short pad of silica gel using dichloromethane as the eluent. The solution was evaporated and the residue was recrystallized from ether-hexane to give 11.5 g (78%) of product, mp 53°-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519062
Source datasetuspto-grants-1996_05
ORD IDord-f7f6b1f60dcd438da49f14dc960421d3
Source noteuspto-grants-1996_05