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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274409Generated: November 1, 2026

Dimethyl Sulfoxide → 4-(7-Chloroquinolin-4-yl)butyraldehyde

https://huagongshe.com/reaction/1274409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(7-Chloroquinolin-4-yl)butan-1-olHCID 22120667—
SolventDichloromethaneHCID 6344—
Product4-(7-Chloroquinolin-4-yl)butyraldehydeHCID 22120673—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Oxalyl chloride (0.42 mL of a 2M solution in dry methylene chloride) was placed in an oven-dried flask, cooled to -78° C. and a solution of 99 mg methylsulfoxide in dry methylene chloride (2 mL) added drop by drop to the oxalyl chloride over 3 minutes and stirred for a further 3 minutes. A solution of 4-(7-chloroquinolin-4-yl)butan-1-ol (100 mg) in dry methylene chloride (1 mL) was added to the reaction flask over approx. 3 minutes followed by anhydrous triethylamine (0.42 mL) and the reaction mixture stirred for another 2.5 hours during which time it was allowed warmed up to room temperature. The reaction was quenched by the addition of saturated brine and then partitioned with methylene chloride. The aqueous layer was discarded and the methylene chloride extract dried over anhydrous sodium sulfate powder, filtered and concentrated in vacuo. The title compound was isolated by flash chromatography on silica gel (ethyl acetate:hexane, 2:1; then ethyl acetate), 57 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156767
Source datasetuspto-grants-2000_12
ORD IDord-cb0d1846999c48b7b3ba7a03c6b96910
Source noteuspto-grants-2000_12