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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198877Generated: November 2, 2026

Triethylamine → 4-Quinolinylmethyl methanesulfonate

https://huagongshe.com/reaction/1198877

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 numberUS04898854
Source datasetuspto-grants-1990_02
ORD IDord-9d71cf4b7b0244e5b9af3d67670fe156
Source noteuspto-grants-1990_02