Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616536Generated: November 1, 2026

Dimethyl Sulfoxide → 7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptanal

https://huagongshe.com/reaction/1616536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptan-1-olHCID 68491411—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product7-[4-(4-Methoxyphenyl)thiazol-2-yl]heptanalHCID 5932407799.4%

Reaction Steps

Add anhydrous dimethyl sulfoxide (0.25 mL, 3.52 mmol) dropwise over 2 minutes to a solution of oxalyl chloride (393 mg, 3.10 mmol) in methylene chloride (10 mL) at −78° C. under nitrogen and stir the mixture for 20 minutes. Add a solution of 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptan-1-ol (0.609 g, 1.99 mmol) in methylene chloride (10 mL) dropwise in 5 minutes and then stir the mixture for 30 minutes. To this mixture, add triethylamine (1.0 mL, 7.2 mmol), stir and warm the reaction mixture to room temperature for 40 minutes. Dilute the mixture with ethyl acetate (100 mL), wash with brine (3×30 mL), dry over sodium sulfate and remove the solvent under reduced pressure to provide 7-[4-(4-methoxyphenyl)thiazol-2-yl]heptanal (0.6 g, 99%): APCI mass spectrum m/z 304 [C17H21NO2S+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765796B2
Source datasetuspto-grants-2014_07
ORD IDord-722a218189f64f02be7d4b8e90c8a7c3
Source noteuspto-grants-2014_07