Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855813Generated: October 27, 2026

Ethanol → 2-(Hydroxymethyl)-6,7-dimethoxy-3-methyl-quinoxaline

https://huagongshe.com/reaction/1855813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2-(Bromomethyl)-6,7-dimethoxy-3-methyl-quinoxalineHCID 23349317—
SolventWaterHCID 962—
Product2-(Hydroxymethyl)-6,7-dimethoxy-3-methyl-quinoxalineHCID 20559638—

Reaction Steps

8.9 g (30 mmols) of 2-(bromomethyl)-6,7-dimethoxy-3-methyl-quinoxaline are suspended in a mixture of 158 g (1.5 mols) of sodium carbonate, 350 ml of water and 100 ml of ethanol. The suspension is boiled under reflux for four hours. 300 ml of water are then added and the resulting mixture is extracted with three times 120 ml of chloroform. The organic phase is dried over magnesium sulphate. The solvent is evaporated in vacuo. The solid residue is recrystallised from methanol. This gives 3.5 g (50%) of a white powder. Melting point: 176° to 177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04216320
Source datasetuspto-grants-1980_08
ORD IDord-9715fba41e894c8581492883f14cdc73
Source noteuspto-grants-1980_08