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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358670Generated: October 30, 2026

Triethylamine → 1-Methyl-4-oxo-1,4-dihydroquinol-3-yl 1-butanesulphonate

https://huagongshe.com/reaction/358670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Butanesulfonyl chlorideHCID 75430—
Reactant4(1H)-Quinolinone, 3-hydroxy-1-methyl-HCID 590078—
SolventDichloromethaneHCID 6344—
Product1-Methyl-4-oxo-1,4-dihydroquinol-3-yl 1-butanesulphonateHCID 23128079—

Reaction Steps

3-Hydroxy-1-methyl-4-quinolone (3 g) was suspended in dichloromethane (200 ml), triethylamine (5.6 ml) was added to the suspension and the mixture was stirred at ambient temperature for hour. 1 -Butanesulphonyl chloride (2.6 ml) was added to the suspension, the mixture stirred for 90 minutes and then left to stand overnight. The resultant mixture was washed with water (400 ml), aqueous sodium hydroxide (1M, 400 ml) and then further water (3×300 ml). The dichloromethane layer was dried over magnesium sulphate and evaporated to give a solid which was crystallised from methanol (100 ml) to give the novel compound 1-methyl-4-oxo-1,4-dihydroquinol-3-yl 1-butanesulphonate, m.p. 143°-144°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997840
Source datasetuspto-grants-1991_03
ORD IDord-fb8da9ab9d124799922b95279e548b65
Source noteuspto-grants-1991_03