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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422896Generated: October 31, 2026

Triethylamine → 6-Methoxy-3-trifluoromethanesulfonyloxy-quinoline-4-carboxylic acid methyl ester

https://huagongshe.com/reaction/1422896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantMethyl 3-hydroxy-6-methoxyquinoline-4-carboxylateHCID 46912076—
SolventDichloromethaneHCID 6344—
Product6-Methoxy-3-trifluoromethanesulfonyloxy-quinoline-4-carboxylic acid methyl esterHCID 8667152876%

Reaction Steps

Trifluoromethanesulfonic anhydride (3.35 mL, 19.94 mmol, 1.5 eq) is added at room temperature to a stirred solution of 3-hydroxy-6-methoxy-quinoline-4-carboxylic acid methyl ester (3.1 g, 13.29 mmol, 1.0 eq) in dichloromethane (30 mL), followed by triethylamine (5.6 mL, 39.88 mmol, 3.0 eq). After 1 hour stirring at room temperature, solvent is removed and the residue is purified by column chromatography (silica gel, eluent: petroleum ether:ethyl acetate, 5:1, v/v) to afford 6-methoxy-3-trifluoromethanesulfonyloxy-quinoline-4-carboxylic acid methyl ester as a yellow solid (3.69 g, 76% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927541B2
Source datasetuspto-grants-2015_01
ORD IDord-43216227d73a4d79ba549cc5b4bfb3d8
Source noteuspto-grants-2015_01