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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647446Generated: October 31, 2026

Dimethyl Sulfoxide → 3-Butyryl-4-(o-tolylamino)quinoline-8-carbaldehyde

https://huagongshe.com/reaction/1647446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Butyryl-4-(2-methylphenylamino)-8-hydroxymethylquinolineHCID 10427010—
SolventDichloromethaneHCID 6344—
Product3-Butyryl-4-(o-tolylamino)quinoline-8-carbaldehydeHCID 1038210282.8%

Reaction Steps

Oxalyl chloride (18.22 g, 0.144 mol) in dichloromethane (180 ml, dried over molecular sieves) was cooled to -70° C., and a solution of dimethylsulphoxide (13.08 g, 0.168 mol) in dry dichloromethane (20 ml) added dropwise under nitrogen with stirring, keeping the temperature below -60° C. After 30 minutes, a solution of 3-butyryl-4-(2-methylphenylamino)-8-hydroxymethylquinoline (40 g, 0.12 mol) in dry dichloromethane (700 ml) was added dropwise below -60° C. After a further 30 minutes, triethylamine (102 ml) was added dropwise, and the mixture allowed to warm to room temperature, washed with water and dried (Na2SO4). The filtered solution was evaporated to a yellow oil, which crystallised on trituration with ether to give the title compound (33.02 g), m.p. 142°-4°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432182
Source datasetuspto-grants-1995_07
ORD IDord-eb183d01d66e4a6ebd1b5c5aff64f2ae
Source noteuspto-grants-1995_07