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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942254Generated: November 3, 2026

Chloroform → 4-Chloro-6,7-bis(2-methoxyethoxy)quinazoline

https://huagongshe.com/reaction/1942254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18925053HCID 18925053—
SolventDimethylformamideHCID 6228—
Product4-Chloro-6,7-bis(2-methoxyethoxy)quinazolineHCID 11289942—

Reaction Conditions

Temperature27.5 °C

Reaction Steps

6,7-Bis(2-methoxy-ethoxy)-quinazolone (68 gm), chloroform (1360 ml) and dimethylformamide (7.5 ml) are taken in a reaction flask at 25-30° C. and stirring begun. To the contents is added oxalyl chloride (120 ml) at 25-30° C. slowly for 30 minutes, which is then heated to reflux for 1 hour 30 minutes. The solvent is distilled at 55-60° C. under vacuum, diisopropyl ether (560 ml) is added, cooled to 25-30° C. and then stirred for 30 minutes. The compound is filtered and washed with diisopropyl ether (100 ml). The compound is added to chloroform (1000 ml), the chloroform is washed two times with 8% NaHCO3 solution (each time 680 ml) and the resulting organic layer is washed with water (500 ml), the organic layer is dried over sodium sulfate and the solvent is distilled under a vacuum at 55-60° C. To the residue is added n-heptane and stirred for 1 hour at 25-30° C. The material, is filtered washed with n-heptane (100 ml) and then the material is dried at 50° C. under vacuum to obtain 65 gm of 4-Chloro-6,7-bis-(2-methoxyethoxy)-quinazoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389531B2
Source datasetuspto-grants-2013_03
ORD IDord-c55d9a2911534b6786c7fb27e934c03d
Source noteuspto-grants-2013_03