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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965001Generated: November 2, 2026

Triethylamine → 7-Methanesulfonylmethyl-4-chloroquinoline

https://huagongshe.com/reaction/965001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Chloroquinolin-7-yl)methanolHCID 22054610—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventAcetone cardiceHCID 18522661—
Product7-Methanesulfonylmethyl-4-chloroquinolineHCID 19075110—

Reaction Steps

7-Hydroxymethyl-4-chloroquinoline (930 mg, 4.82 mmol) dissolved in anhydrous methylene chloride (40 ml) was added with triethylamine (679 mg, 6.72 mmol). The mixture was cooled in dry ice/acetone bath, added dropwise with methanesulfonyl chloride (770 mg, 6.7 mmol) and the reactant was stirred for 20 minutes without the cooling bath. Then, the reactant was added under ice-water cooling with cool aqueous solution of saturated sodium bicarbonate (40 ml) and ethyl acetate (150 ml) and shaken to separate the organic layer. The separated organic layer was washed with saturated saline solution and dried over magnesium sulfate. The solvent was removed to obtain 7-methanesulfonylmethyl-4-chloroquinoline as oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773449
Source datasetuspto-grants-1998_06
ORD IDord-dd8a4311f2744953aaa33480d6579f42
Source noteuspto-grants-1998_06