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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193274Generated: October 30, 2026

Dimethyl Sulfoxide → HCID 59398316, compound

https://huagongshe.com/reaction/2193274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 59398261HCID 59398261—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
ProductHCID 59398316HCID 59398316—

Reaction Steps

To 5 mL of a dichloromethane solution containing 0.11 mL of oxalyl chloride, 0.22 mL of dimethylsulfoxide was added dropwise under nitrogen atmosphere at −60° C., and stirred for 10 min. 20 mL of a dichloromethane solution containing 0.23 g of 1-(2-hydroxyethyl)-4-methoxyquinolin-2(1H)-one was added dropwise at the same temperature, and stirred for 10 min. After 0.58 mL of triethylamine was added at the same temperature, it was stirred at room temperature for 1.5 hours, and water was added. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and extracts were combined, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give (4-methoxy-2-oxoquinolin-1(2H)-yl)acetaldehyde as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329694B2
Source datasetuspto-grants-2012_12
ORD IDord-6fb54f547af14d49bb15d960b845af07
Source noteuspto-grants-2012_12