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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617124Generated: October 26, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 3-[4-(2-Chloro-ethoxy)-phenyl]-7-methoxy-2-(4-methoxy-phenyl)-3H-quinazolin-4-one

https://huagongshe.com/reaction/617124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
Reactant3-[4-(2-chloro-ethoxy)-phenyl]-7-methoxy-2-(4methoxy-phenyl)-2,3-dihydro-1H-quinazolin-4-oneHCID 21851080—
SolventTolueneHCID 1140—
Product3-[4-(2-Chloro-ethoxy)-phenyl]-7-methoxy-2-(4-methoxy-phenyl)-3H-quinazolin-4-oneHCID 21851082—

Reaction Steps

To a solution of 8.1 g (0.0185 mol) of 3-[4-(2-chloro-ethoxy)-phenyl]-7-methoxy-2-(4methoxy-phenyl)-2,3-dihydro-1H-quinazolin-4-one in 300 mL of toluene was added 4.2 g (0.0185 mol) of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone. The reaction mixture was stirred and heated to reflux for 2 hours. The toluene was removed in a rotary evaporator. Ethanol (300 mL) was added to the reaction flask which was allowed to stir at room temperature overnight. The precipitate was collected by vacuum filtration and amounted to 6.9 g. The product (mp 186-187° C.) was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948775
Source datasetuspto-grants-1999_09
ORD IDord-12d5ef3893d249eab44ce3cbcbe16c21
Source noteuspto-grants-1999_09