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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587303Generated: November 3, 2026

Triethylamine → 4-Quinolinylmethyl methanesulfonate

https://huagongshe.com/reaction/1587303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(Hydroxymethyl)quinolineHCID 80479—
SolventDichloromethaneHCID 6344—
Product4-Quinolinylmethyl methanesulfonateHCID 13540821—

Reaction Steps

A solution of methanesulfonyl chloride (4.84 ml) in 20 ml of methylene chloride is slowly added over 20 minutes to a solution of 8.29 g of 4-hydroxymethylquinoline and 11 ml of triethylamine in 200 ml of methylene chloride at 0°. After completion of the reaction at room temperature, the reaction mixture is partitioned between methylene chloride and saturated potassium carbonate solution. The organic layer is dried over sodium sulfate and evaporated to dryness to yield 4-(methanesulfonyloxymethyl)quinoline as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217963
Source datasetuspto-grants-1993_06
ORD IDord-e56776b78a4a4930a74bff08a1394a2d
Source noteuspto-grants-1993_06