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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387644Generated: October 29, 2026

Water → 5-bromo-2-(2-methoxyethyl)-3,4-dihydroisoquinolin-1(2H)-one

https://huagongshe.com/reaction/387644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant5-bromo-2-(2-hydroxyethyl)-3,4-dihydroisoquinolin-1(2H)-oneHCID 68473635—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product5-bromo-2-(2-methoxyethyl)-3,4-dihydroisoquinolin-1(2H)-oneHCID 21865471—

Reaction Steps

0.39 g of 5-bromo-2-(2-hydroxyethyl)-3,4-dihydroisoquinolin-1(2H)-one is dissolved under an inert atmosphere in 3 cm3 of dimethylsulfoxide at a temperature close to 20° C. 105 mg of finely ground potassium hydroxide are added. The reaction mixture is stirred for 30 min at a temperature close to 20° C., then 0.108 cm3 of iodomethane is introduced. The stirring is continued for 20 h at a temperature close to 20° C. 30 cm3 of water and 30 cm3 of ethyl ether are added. After decanting, the organic phase is washed with 30 cm3 of a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated using a rotary evaporator under reduced pressure (5 kPa). 170 mg of 5-bromo-2-(2-methoxyethyl)-3,4-dihydroisoquinolin-1(2H)-one are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372864B2
Source datasetuspto-grants-2013_02
ORD IDord-756d84f986ff42e19c47b87ae9739399
Source noteuspto-grants-2013_02